| Different patterns of X chromosome inactivity in lymphocytes and fibroblasts of a human balanced X; autosome translocation |
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| De novo mutations producing unstable Hbs or Hbs M. |
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| Cytogerontology since 1881: A reappraisal of August Weismann and a review of modern progress |
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| The genetic linkage between the PKU locus and the loci for Amylase1, Amylase2, Fy, PGM1, and Rh and the question of assignment of the PKU locus to chromosome No. 1 |
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| Distamycin A-DAPI banding of nonfluorescent Y (Ynf) chromosomes in 45,X/46,XYnf mosaicism |
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| Nonfluorescent Y chromosomes. Cytologic evidence of origin |
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| Exclusion of linkage between the loci for multiple endocrine neoplasia type-2 (MEN-2) and HLA |
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| Diagnosis of Hunter's syndrome carriers; Radioactive sulphate incorporation into fibroblasts in the presence of fructose 1-phosphate |
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| Centric fission of chromosome No. 7 in three generations |
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| Cryptorchidism and hypogenitalism in X-linked recessive ichthyosis vulgaris |
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| Tangier disease: Heterozygote detection and linkage analysis |
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| Human ?-galactosidase and ?-neuraminidase deficient mucolipidosis: Genetic complementation analysis of the neuraminidase deficiency |
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| X-linked genes of the H-Y antigen system in the wood lemming (Myopus schisticolor) |
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| Retinoblastoma in a boy with a de novo mutation of a 13/18 translocation: The assumption that the retinoblastoma locus is at 13q141, particularly at the distal portion of it |
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| Cytogenetic studies of a family with trisomy 21 mosaicism in two successive generations as the cause of Down's syndrome |
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| Of rabbit and man: Comparative gene mapping |
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| Glucose-6-phosphate dehydrogenase deficiency in Papua New Guinea |
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| The crucial band for phenotype of trisomy 18 |
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| An attempt to define 1qh+, 9qh+, and 16qh+ |
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| Genetic variants of placental alkaline phosphatase as detected by a monoclonal antibody |
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| Genetic analysis of human lymphocyte proteins by two-dimensional gel electrophoresis: 2. Genetic polymorphism of lymphocyte cytosol 64K polypeptide |
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| Ovarian development in 46,XY gonadal dysgenesis |
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| Genetic aspects of nonchromaffin paraganglioma |
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| Five new Gc variants detected by isoelectric focusing in agarose gel |
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| Meiotic and synaptonemal complex studies in 45 subfertile males |
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| Peculiar findings in a family with keratodermia palmo-plantaris papulosa buschke-fischer-brauer |
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| Intracellular phenylalanine and tyrosine concentration in homozygotes and heterozygotes for phenylketonuria (PKU) and hyperphenylalaninemia compared with normals |
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| A simple reproducible method for prometaphase chromosome analysis |
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| Idiopathic hemochromatosis: demonstration of homozygous-heterozygous mating by HLA typing of families |
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| Transferrin C subtyping in Malaysians and in Indonesians from North Sumatra |
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| Chromosome abnormalities involving 11p13 and low erythrocyte catalase activity |
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| Roberts' ? SC phocomelia syndrome with cytogenetic findings |
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| Del(5p) without ?cri du chat? phenotype |
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| Homocystinuria |
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| Genetic control of human apolipoprotein E polymorphism: Comparison of one-and two-dimensional techniques of isoprotein analysis |
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| Altered frequency of initiation sites of DNA replication in Werner's syndrome cells |
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| Yqs in an American family of Scottish Descent |
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Scottish Descent |
| Incidence of Hunter's syndrome |
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| Cell morphology in long-term cultures of normal and abnormal amniotic fluids |
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| Fragile site Xq27 and mental retardation. Clinical and cytogenetic manifestation in heterozygotes and hemizygotes of five kindreds |
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| Polymorphisms of Ag-stained nucleolar organizer regions in man |
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| The effect of aphidicolin on the rate of DNA replication and unscheduled DNA synthesis of Bloom syndrome and normal fibroblasts |
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| Causes of chromosome anomalies suggested by cytogenetic epidemiology of induced abortions |
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| Sexual behaviour is independent of H-Y antigen constitution |
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| Investigation of genetic markers in a true Hermaphrodite with chi 46,XX/46,XY |
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| Pyruvate kinase ?G�ttingen1,2?: Congenital hemolytic anemia, evidence of double heterozygosity, and lack of enzyme cooperativity |
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| Transmission of fragile (X)(q27) from normal male(s) |
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| Diphenoloxidases in various forms of myopathy which are transmitted by different genetic mechanisms |
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| Cytogenetic toxicity of antitumor platinum compounds in Fanconi's anemia |
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| The mode of inheritance of ovalocytosis/elliptocytosis in Malaysian Orang Asli families |
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| A red cell pyruvate kinase mutant with normal L-type PK in the liver |
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| Interstitial deletion 46,XY,del(1)(q23q25) |
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| Population genetical aspects of primary congenital glaucoma. I. Incidence, prevalence, gene frequency, and age of onset |
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| Population genetic aspects of primary congenital glaucoma. II. Fitness, parental consanguinity, founder effect |
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| Polymorphism of the haptoglobin peptides by isoelectric focusing electrophoresis and isoelectric point determinations |
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| Prenatal diagnosis and outcome of pregnancy in 2036 women investigated by amniocentesis |
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| Somatic cell hybridization studies on the genetic regulation and allelic mutations in metachromatic leukodystrophy |
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| Interphase flow-cytogenetics: Correlation of DNA fluorescence to aneuploidy in human fibroblast cultures |
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| Lack of effect of vitamin C on the incidence of chromosome anomalies induced by influenza virus in germ cells of mice |
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| Homozygous Robertsonian translocations in a fetus with 44 chromosomes |
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| Detection of carriers for duchenne muscular dystrophy. Quality control of creatine kinase assay |
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| Lethal, neonatal, short-limbed platyspondylic dwarfism. A further variant? |
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| A new case of satellited Yq chromosome |
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| Announcements |
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| Similar chromosomal abnormalities in several retinoblastomas |
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| Analysis of the breakpoints in translocation (15;17) Observed in 4 patients with acute promyelocytic leukemia |
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| The DNA tumor virus SV 40 induces gene mutations in human cells. Reversion of HPRT deficiency |
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| Isoelectric focusing of human red cell phosphoglucomutase (PGM1). Phenotype distribution in the population of Tuscany and two hereditary variants |
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✓ |
|
population of Tuscany |
| The expression of fragile X chromosomes in members of the same family at different times of examination |
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| Deletion of 13q in two patients with retinoblastoma, one probably due to 13q- mosaicism in the mother |
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| Dentition of a 48,XYY,+21 male |
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| Nondisjunction and chromosome breakage in mouse oocytes after various X-ray doses |
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| A variant of the fra(X) syndrome |
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| The phenotype in de novo and familial pericentric inversion 6. A problem in karyotype-phenotype correlation |
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| G-6-PD Guadalajara. A new mutant associated with chronic nonspherocytic hemolytic anemia |
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| Pairing of X and Y chromosomes, non-inactivation of X-linked genes, and the maleness factor |
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| Higher inductions of twin and single sister chromatid exchanges by cross-linking agents in Fanconi's anemia cells |
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| Quantitative studies on the arrangement of human metaphase chromosomes |
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| Distal 19q duplication |
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| Confirmation of regional assignment of gene for human esterase-D to chromosome band 13q14 |
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| First announcement |
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| Genetic homology and crossing over in the X and Y chromosomes of mammals |
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| High rate of detection of 13q14 deletion mosaicism among retinoblastoma patients (using more extensive methods) |
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| Muscle provocation test. A sensitive method for discrimination between carriers and noncarriers of Duchenne muscular dystrophy |
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| Cytogenetic investigations in 150 cases with complaints of sterility or primary amenorrhea |
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| Three new rare variants of ?1-Antitrypsin |
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| Giemsa-11 technique. Applications in the chromosomal characterization of hematologic specimens |
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| Gm and Km immunoglobulin allotypes in Reindeer Chukchi and Siberian Eskimos |
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| Well-identifiable human chromosomes Isolated from mitotic fibroblasts by a new method |
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| Standardization of nomenclature for transcobalamin II variants |
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| Chromosome 17 has a real fragile site at p12 |
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| Segregation analysis of ?-L-fucosidase activity |
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| Direct versus cultured preparation of bone marrow cells from 22 patients with acute myeloid leukemia |
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| Absence of linkage between the serum cholinesterase (CHE1) and rhesus (RH) loci |
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| The genetic polymorphism of ?-aminolevulinate dehydrase in Italy |
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| Extra band in the 9qh+ chromosome in a normal father and in his child with multiple congenital anomalies |
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| Erratum |
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| Complete moles have paternal chromosomes but maternal mitochondrial DNA |
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| Gm and Km frequencies in a Portugese population |
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| On the frequency of telomeric chromosomal changes induced by culture conditions suitable for fragile X expression |
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| Assignment of human uroporphyrinogen I synthase locus to region 11qter by gene dosage effect |
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| Sister chromatid exchanges in leukocytes of patients with cancer of cervix uteri |
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| Heterogeneity of ?Mediterranean type? glucose-6-phosphate dehydrogenase (G6PD) deficiency in Spain and description of two new variants associated with favism |
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|
✓ |
|
Mediterranean; Spain |
| The mendelian inheritance of a human X chromosome-specific DNA sequence polymorphism and its use in linkage studies of genetic disease |
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| Cytogenetic abnormalities in a patient with hypercalcemia and papillary thyroid carcinoma |
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| 46,XY/47,XY,+17 mosaicism in a newborn with severe malformations |
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| H-Y antigen in male patients with X polysomies |
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| Functional assessment of genetic variants of ?1-Antitrypsin |
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| Editorial help |
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| Regional mapping of the locus for hexokinase-1 (HK1) to 10p11?q23 by gene dosage in human fibroblasts |
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| The central localization of the small and early replicating chromosomes in human diploid metaphase figures |
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| The cincinnati lipid research clinic family study: Familial determinants of plasma uric acid |
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| Flow cytometric characterization of a Chinese hamster x man hybrid cell line retaining the human Y chromosome |
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| Failure to detect polycystic kidneys in utero by second trimester ultrasonography |
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| Identification and function of serologically detectable H-Y antigen |
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| The HLA-A:HLA-B crossovers and their contribution in analysing possible haplotype-specific recombination rates |
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| Correlation between the number of sex chromosomes and the H-Y antigen titer |
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| An excess of the Pi Sallele in dizygotic twins and their mothers |
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|
| Werner's syndrome: A review of recent research with an analysis of connective tissue metabolism, growth control of cultured cells, and chromosomal aberrations |
|
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|
| Clonal structural chromosomal rearrangements in primary fibroblast cultures and in lymphocytes of patients with Werner's syndrome |
|
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|
| Familial lecithin-cholesterol acyltransferase deficiency in a Japanese family: Evidence for functionally defective enzyme in homozygotes and obligate heterozygotes |
|
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|
| Homologous early replication patterns of the distal short arms of prometaphasic X and Y chromosomes |
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| Replication pattern in XXY cells with fra(X) |
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|
| Five cases of prenatally detected true mosaic trisomy 20 |
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| Macroorchidism and fragile X in mentally retarded males |
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| Cocultivation studies with cells of patients bearing fragile X chromosomes |
|
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|
| High prevalence of Werner's syndrome in Sardinia. Description of six patients and estimate of the gene frequency |
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| X-Linked Leigh's syndrome |
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| Abnormal blood group galactosyltransferase in blood type A1B-subjects whose sera contain anti-B agglutinin |
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| Announcements |
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| A simplified procedure for haptoglobin subtyping |
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| Letter to the editors |
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| The dermatoglyphic and clinical features of the 9p trisomy and partial 9p monosomy syndromes |
|
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| Pathogenetic significance of ?pure? monosomy 7 in myeloproliferative disorders. analysis of 14 cases |
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| Glyoxalase I polymorphism and racial admixture in the Cuban population |
|
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|
✓ |
|
racial admixture; Cuban population |
| The turner phenotype and the different types of human X isochromosome |
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| Incidence of chromosome abnormalities in newborn children. Comparison between incidences in 1969?1974 and 1980?1982 in the same area |
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| Relationship between behavioral maturation measured by the ?Baum? test and EEG frequency. A pilot study on monozygotic and dizygotic twins |
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|
| Evidence for the deficiency of ?-glucosidase-activating factor in fibroblasts of patients with I-cell disease |
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| Sperm aging in the male and cytogenetic anomalies. An animal model |
|
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| The isochromosome (17q) in chronic myelocytic leukaemia: Mechanism of origin, centromeric function and clonal evolution |
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| Familial neurofibromatosis and juvenile chronic myelogenous leukemia |
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| Erratum |
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|
| Polymorphism of BF, C2, and GLO in Japanese patients with insulin-dependent diabetes mellitus: Confirmation of an increase of BF *FT |
|
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|
|
| Pericentric X inversion in dizygotic twins who differ in X chromosome inactivation and menstrual cycle function |
|
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|
|
| The locus for apolipoprotein E (apoE) is linked to the complement component C3 (C3) locus on chromosome 19 in man |
|
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|
| Translocation(X;Y)(p22.33;p11.2) in XX males: Etiology of male phenotype |
|
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|
|
| Meiotic chromosomes in a female with primary trisomic Down's syndrome |
|
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|
|
| Prenatal detection of a fetus hemizygous for the fragile X-chromosome |
|
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| Repeated anencephaly and XO/XX mosaicism in the mother |
|
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|
| Langer-Giedion syndrome with and without del 8q. Assignment of critical segment to 8q23 |
|
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|
| Glycoproteins that distinguish different cell types found in amniotic fluid |
|
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|
| Transmission of the PiZ allele for ?1-antitrypsin deficiency: Population genetic considerations |
|
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|
|
| Clastogenic effect of the psychotropic drug thioridazine on human chromosomes in vivo |
|
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|
| Analysis of chromosome positions in the interphase nucleus of Chinese hamster cells by laser-UV-microirradiation experiments |
|
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|
|
| Analysis of linkage relationships in maturity-onset diabetes of young people and independent segregation of C6 and HLA |
|
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|
| Polymorphism of human chromosomes 1, 9, 16, Y: Variations, segregation and mosaicism |
|
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|
| Fetal cells in the maternal circulation: Detection by direct AFP-immunofluorescence |
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| Male infertility in a case of (Y;6) balanced reciprocal translocation. Mitotic and meiotic study |
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|
| Endomitosis in human trophoblast |
|
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| RHG-band polymorphism of the short arms of human acrocentric chromosomes and relationship of variants to satellite associations |
|
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|
|
| The Meckel syndrome. Pathological and cytogenetic observations in eight cases |
|
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|
| A rare phenotype of phosphoglucomutase-2 first detected in Mongoloids |
|
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|
|
|
✓ |
|
Mongoloids |
| Genetic hemoglobin abnormalities in 2363 Cuban newborns |
|
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|
|
| Human chromosomal polymorphism. III. Chromosomal Q polymorphism in Mongoloids of northern Asia |
|
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|
|
|
✓ |
|
Mongoloids |
| Human chromosomal polymorphism. IV. Chromosomal Q polymorphism in Russians living in Kirghizia |
|
|
|
|
|
|
✓ |
|
Russians living in Kirghizia |
| Human chromosomal polymorphism. V. Chromosomal Q polymorphism in African populations |
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| Data and theory for a revised chiasma map of man |
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| Gene mapping and serendipity. The locus for torticollis, keloids, cryptorchidism and renal dysplasia (31430, McKusick) is at Xq28, distal to the G6PD locus |
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| Replication status of the fragile X chromosome, fra(X)(q27), in three heterozygous females |
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| Determination of the H-Y antigen in amniotic cells. Its use in prenatal diagnosis |
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| The human genetic mutant cell repository |
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| Sister chromatid exchanges and structural chromosome aberrations in relation to age and sex |
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| Mirror image duplications of chromosome 21. Three new cases and discussion of the mechanisms of origin |
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| Ring 18 mosaicism in identical twins |
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| Partial trisomy for the long arm of chromosome 7. Case report and review |
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| A syndrome of midface retraction, multiple radiological anomalies, renal malformations and hypertrichosis |
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| Quantitative studies on the arrangement of human metaphase chromosomes. IX. Arrangement of chromosomes with and without spindle apparatus |
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| Assignment of the structural gene coding for albumin to human chromosome 4 |
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| Four patients including two sisters with the acrocallosal syndrome (Agenesis of the corpus callosum in combination with preaxial hexadactyly) |
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| Epistatic association and linkage analysis in human families |
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| Analysis of heterogeneity in Fanconi's anemia patients of different ethnic origin |
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| Patterns of exchange induced by mitomycin C in C-bands of human chromosomes. II. High frequency of Y-Y exchange in XYY cells |
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| Expression of fra(X)(q28) is Suppressed in man-mouse hybrid cells |
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| Deficiency of coagulation factors VII and X associated with deletion of a chromosome 13 (q34). Evidence from two cases with 46,XY,t(13;Y)(q11;q34) |
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| A possible new locus of alkaline phosphatase expressed in human testis |
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| Specfic staining of 9h in human somatic interphase cells by D 287/170 |
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| Trisomy 21: Origin of non-disjunction |
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| Extracentromeric connections between sister chromatids demonstrated in human chromosomes induced to condense asymmetrically |
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| The cell cycle of lymphocytes in Fanconi anemia |
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| Biochemical and genetic characterization of the lowell variant. A new phenotype of 6-phosphogluconate dehydrogenase |
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| Patterns of exchange induced by mitomycin C in C-bands of human chromosomes. I. Relationship to C-band size in chromosomes 1, 9, and 16 |
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| Apolipoprotein A-IV polymorphism in man |
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| Karyotyping chromosomes by electron microscopy. II. A method for the sequential examination of spread and banded metaphases by light and electron microscopy |
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| A new glucose-6-phosphate dehydrogenase variant (G6PD Nagano) associated with congenital hemolytic anemia |
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| Tetraploid conceptus with three paternal contributions |
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| Crossing-over during human spermatogenesis visualized cytologically |
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| Genetic determination of NOR activity in human lymphocytes from twins |
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| Controlled trial of serum isoelectric focusing in the detection of the cystic fibrosis gene |
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| Genetic polymorphism of human plasminogen in the Japanese population: New plasminogen variants and relationship between plasminogen phenotypes and their biological activities |
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| Cytogenetic findings in 4952 prenatal diagnoses. An Italian collaborative study |
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| Elevated levels of arylsulfatase C activity in cultured skin fibroblasts of patients with autosomal dominant ichthyosis vulgaris |
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| Maternally transmitted extra ring(21) chromosome in a boy with Down's syndrome |
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| The ring chromosome 13 syndrome |
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| Support for random alignment of mitotic chromatids in associating nucleolus organizers |
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| Improved typing of human serum transferrin by isoelectric focusing on ultrathin layer polyacrylamide slab gels |
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| Blood group, protein, and red cell enzyme polymorphisms of the Hadza of Tanzania |
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| Familial pericentric inversion of chromosome 1 in a boy with Goldenhar's syndrome |
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| Genetic control of H-Y synthesis. A hypothesis |
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| Prometaphase banding of human chromosomes with basic fuchsin |
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| Partial Turner's syndrome in four girls with Xq duplication and Xp deficiency |
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| Fibrinogen γ chain locus is on chromosome 4 in man |
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| Mosaic trisomies in human spontaneous abortions |
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| Glyoxalase I polymorphism and racial admixture in the Cuban population |
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✓ |
|
racial admixture; Cuban population |
| Apparent homozygosity for the fragile site at Xq28 in a normal female |
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| High resolution banding of prometaphase chromosomes |
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| Chromosome breakage factor in the plasma of two Bloom's syndrome patients |
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| Comparison of two measuring methods for the evaluation of C-heterochromatin in human chromosomes |
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| Increased sister chromatid exchanges in epileptic children during long-term therapy with phenytoin |
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| Colchicine resistance in human cell lines. Pleiotropic phenotype and decreased membrane permeability |
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| Alpha-1-antitrypsin (?1AT) phenotypes and PiM subtypes in Italy. Evidence of considerable geographic variability |
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| Unusually early dividing chromosomes 13?15 in a child with retinoblastoma and 13q delection |
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| Translocation t(X;1) and the ?critical region hypothesis? |
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| Increase in the incidence of the fragile site Xq27 in prometaphases |
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| Erratum |
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| An XX male with a 46,XX/47,XX,+Y(q12?qter) karyotype |
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| Duplication of the short arm of chromosome 9. Analysis of five cases |
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| Genetics of complement C4. Two homoduplication haplotypes C4S C4S and C4F C4F in a family |
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| The study of X-rays and TCDD effects on satellite associations may suggest a simple model for application in environmental mutagenesis |
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| Aminolevulinate dehydratase (E.C. 4.2.1.24): Linkage analysis |
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| Partial inversion of the secondary constriction of chromosome 9: It exists |
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| First announcement of the Fanconi anemia International Registry |
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| Human chromosomal polymorphism. I. Chromosomal Q polymorphism in Mongoloid populations of central Asia |
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✓ |
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Mongoloid |
| Assigning the polymorphic human insulin gene to the short arm of chromosome 11 by chromosome sorting |
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| Distinction �lectrophor�tique entre les deux sous-esp�ces d'Orang-outan |
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| Variation in the sensitivity of human lymphocttes to DNA-damaging agents measured by sister chromatid exchange frequency |
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| Polymorphism of properdin factor B in Japanese. Description of a rare variant and data of association with HLA and C2 |
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| Announcements |
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| Announcements |
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| Human chromosomal polymorphism. II. Chromsomal C polymorphism in Mongoloid populations of central Asia |
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✓ |
|
Mongoloid |
| A distinct osteochondrodysplasia with hypertrichosis?Individualization of a probable autosomal recessive entity |
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| Rabl's model of the interphase chromosome arrangement tested in Chinise hamster cells by premature chromosome condensation and laser-UV-microbeam experiments |
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| Glucose 6-phosphate dehydrogenase variants of Bali Island (Indonesia) |
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| HLA typing in a new family with fletcher factor deficiency |
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| Cytogenetic studies in a Y-to-X translocation observed in three members of one family, with evidence of infertility in male carriers |
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| Erratum |
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| Evidence for duplication of the human salivary amylase gene |
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| Moderate Down's syndrome in three siblings having partial trisomy 21q22.2?qter and therefore no SOD-1 excess |
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| Methods of increasing the visibility of fragile X chromosomes |
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| Ring chromosome 2: Clinical, chromosomal, and biochemical aspects |
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| Aspects of evaluation, significance, and evolution of human C-band heteromorphism |
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| Bisatellited dicentric chromosome: A report on a case with karyotype 47,XY,+psu dic(22)t(22;22)(22pter?cen?22q11::22q11?22pter) |
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| Apolipoprotein AIMarburg: Studies on two kindreds with a mutant of human apolipoprotein AI |
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| Within pair differences of human chromosome 9 C-bands associated with reproductive loss |
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| X-Autosome translocations: Cytogenetic characteristics and their consequences |
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| Variation �lectrophor�tique et sp�ciation chez les diff�rentes esp�ces de singes anthropo�des |
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| Rates of trisomies 21, 18, 13 and other chromosome abnormalities in about 20 000 prenatal studies compared with estimated rates in live births |
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| Red blood cell sorbitol dehydrogenase deficiency in a family with cataracts |
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| Position of chromosomes in the human interphase nucleus |
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| Factor B polymorphism in North American Blacks: Study of a new variant Bf F1.35 |
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✓ |
|
North American Blacks |
| Agenesis of corpus callosum, ocular, and skeletal anomalies (X-linked dominant aicardi's syndrome) in a girl with balanced X/3 translocation |
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| The Roberts syndrome |
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| Letter to the Editors |
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| Nonspecific X-linked mental retardation?A review |
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| G6PD-Puerto Lim�n: A new deficient variant of glucose-6-phosphate dehydrogenase associated with congenital nonspherocytic hemolytic anemia |
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| Tiny interstitial duplication of proximal 7q in association with a maternal paracentric inversion |
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| Mapping the ?-globin genes in HB J Mexico carriers |
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| Intracellular distribution of DNA topoisomerase I in fibroblasts from patients with Fanconi's anaemia |
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| Study on segregation of the inversion of chromosome 4 (p15.2q11) in two unrelated families |
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| Polymorphism of the Hinf I restriction site located 1 Kb 5? to the human ?-globin gene |
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| Hereditary retinoblastoma: Lack of maternal effect |
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| Parental origin of chromosome abnormalities in spontaneous abortions |
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| Seasonality of pre-ovulatory non-disjunction and the aetiology of Down syndrome. A European collaborative study |
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|
✓ |
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|
A European collaborative study |
| PI (?1-antitrypsin) subtypes: Frequency of PI*M4 in several populations |
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| Genetic analysis of human lymphocyte proteins by two-dimensional gel electrophoresis: 4. Genetic polymorphism of cytosol 100k polypeptide |
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| Distribution of physiological adult lactase phenotypes, lactose absorber and malabsorber, in Germany |
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| Distribution of human adult lactase phenotypes in the population of Austria |
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| Frequency of the ESD*5 allele in three ethnic groups in Minnesota |
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| Paternal age and Down's syndrome genotypes diagnosed prenatally: No association in New York State data |
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| A Hind III restriction site polymorphism in the human collagen ?1(I)-like gene on chromosome No. 7 |
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| Letters to the Editors |
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| Genetic analysis of human lymphocyte proteins by two-dimensional gel electrophoresis: 3. Frequent occurrence of genetic variants in some abundant polypeptides of PHA-stimulated peripheral blood lympho |
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| A foetal alpha-1 antitrypsin which resembles PI*I |
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| Regional mapping of the locus for hexokinase-1 (HK1) |
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