Human Genetics - 1989

295 articles | Last updated: 2025-12-03 14:12:56
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T A T A T A T A
Localization of human c-mos to chromosome band 8q11 in leukemic cells with the t(8;21) (q22;q22)
Detection of single-copy genes by nonisotopic in situ hybridization on human chromosomes
Regional localization and molecular characterization of a DNA sequence on the long arm of chromosome 22
Genotyping of mitochondrial aldehyde dehydrogenase in blood samples using allele-specific oligonucleotides: comparison with phenotyping in hair roots
Myotonic dystrophy is closely linked to the gene for muscle-type creatine kinase (CKMM)
Detection of 1q polysomy in interphase nuclei of human solid tumors with a biotinylated probe
Gene of X-chromosomal congenital stationary night blindness is closely linked to DXS7 on Xp
Fragile sites and statistics
Investigations of chorionic villi after chorionic villus sampling (CVS)
Molecular deletion patterns in Duchenne and Becker type muscular dystrophy
Rapid isolation of moderate and highly polymorphic DNA fragments mapping close to WT (Wilms' tumour) and AN2 (aniridia) on chromosome 11
Study of a family with a fragile site of the X chromosome at Xq27–28 without mental retardation
Molecular genetic diagnosis of sickle cell disease using dried blood specimens on blotters used for newborn screening
Mutation analysis of β-thalassemia genes in a German family reveals a rare transversion in the first intron
Induction of the fragile X on BrdU-substituted chromosomes with direct visualization of sister chromatid exchanges on banded chromosomes
Confirmation and refinement of the localisation of the c-MEL locus on chromosome 19 by physical and genetic mapping
Segregation frequency in microcephaly
A new polymorphic DNA probe pS43 derived from a flow sorted library is assigned to human chromosome 20q13
A severe autosomal recessive acromesomelic dysplasia, the Hunter-Thompson type, and comparison with the Grebe type
Mild hemophilia A resulting from Arg-to-Leu substitution in exon 26 of the factor VIII gene
Cytogenetic analysis of in vitro fertilization (IVF) failures
DNA haplotype analysis at the phenylalanine hydroxylase locus in the Turkish population Turkish population
A proposed growth regulatory function for the serologically detectable sex-specific antigen H-Ys
Isolation of chromosome-21-specific DNA probes and their use in the analysis of nondisjunction in Down syndrome
Hypohidrotic ectodermal dysplasia
Localization of the coagulation factor XIII B subunit gene (F13B) to chromosome bands 1q31?32.1 and restriction fragment length polymorphism at the locus
Detection of Duchenne muscular dystrophy carriers by dosage analysis using the DMD cDNA clone 8
Localization of Y chromosome sequences and X chromosomal replication studies in XX males
Confirmation of linkage disequilibrium between haplotype B (XV-2c, allele 1; KM-19, allele 2) and cystic fibrosis allele in the French population
Familial transmission of 16p trisomy in an infant
Recombination between DXS7, DXS84 and a rare form of X-linked retinitis pigmentosa (McK-30 320)
A genetic and anthropological study of atlanto-occipital fusion
Ferritin H gene polymorphism in idiopathic hemochromatosis
Centromeric association of a microchromosome
Centromeric association and non-random distribution of centromeres in human tumour cells
Chromosomal assignment of a glutamic acid transfer RNA (tRNAGlu) gene to 1p36
Chronic nonspherocytic hemolytic anemia (CNSHA) and glucose 6 phosphate dehydrogenase (G6PD) deficiency in a patient with familial amyloidotic polyneuropathy (FAP)
Ataxia-telangiectasia fibroblasts have less fibronectin mRNA than control cells but have the same levels of integrin and ?-actin mRNA
The human cytochrome P450 CYP3 locus: assignment to chromosome 7q22-qter
H-Y antigenicity of human fibroblasts
Erythrocyte acid phosphatase (ACP1) activity
Presymptomatic testing for Huntington's disease
Sublocalization of the human protein C gene on chromosome 2q13?q14
A new rare PGD variant, PGD Mediterranean
The gene for the Lp(a)-specific glycoprotein is closely linked to the gene for plasminogen on chromosome 6
Phytanic acid alpha-oxidation and complementation analysis of classical Refsum and peroxisomal disorders
The polymerase chain reaction: an improved method for the analysis of nucleic acids
Multiple mutations underlying familial hypercholesterolemia in the South African population
Erratum
Prenatal diagnosis of genetic disorders in preimplantation embryos: invasive and non-invasive approaches
Cystic fibrosis in Finland: a molecular and genealogical study
Assignment of human desmin gene to band 2q35 by nonradioactive in situ hybridization
BamHI and SacI RFLPs of the human immunoglobulin IGHG genes with reference to the Gm polymorphism in African people African people
Fibroblast-specific common fragile sites induced by aphidicolin
Partial correction of chromosome instability in Fanconi anemia by desferrioxamine
Risks of fetal cystic fibrosis based on linkage disequilibrium data
Autosomal dominant polycystic kidney disease and ??4.2 thalassemia in a Caucasian family
Selection of human chromosome 21-specific DNA probes for genetic analysis in Alzheimer's dementia and Down syndrome
Assignment of anonymous DNA probes to specific intervals of human chromosomes 16 and X
A novel ?� arising from a frameshift insertion, detected by direct sequencing of enzymatically amplified DNA
Cytogenetic investigations in a family with ataxia telangiectasia
Detection of an unbalanced translocation (4;14) in a mildly retarded father and son by flow cytometry
Detection of an alteration of the ?2 gene in a patient with chronic lung disease and serum ?2 deficiency
Linkage analyses of human peptidase C (PEPC), human factor H (HF), and coagulation factor XIIIB (F13B)
Announcements
How does inactivation change timing of replication in the human X chromosome?
Long-range restriction map of a region of human chromosome 19 containing the apolipoprotein genes, a CLL-associated translocation breakpoint, and two polymorphic MluI sites
Molecular analysis of 46,XY females and regional assignment of a new Y-chromosome-specific probe
Somatic pairing of chromosome 1 centromeres in interphase nuclei of human cerebellum
Population bottlenecks in Polynesia revealed by minisatellites
Not all chromosome imbalance resulting from the 11q;22q translocation is due to 3:1 segregation in first meiosis
Heterogeneity of mRNA expression in Italian fucosidosis patients
Investigation of the ?variable spreading? of X inactivation into a translocated autosome
The frequency and origin of the sickle cell mutation in the district of Coruche/Portugal
Frequency of heterozygous complete hydatidiform moles, estimated by locus-specific minisatellite and Y chromosome-specific probes
Four variants of human plasma ?2-glycoprotein (ZAG) in the Japanese population
Pure partial trisomy of the short arm of chromosome 5
X-Chromatin fluorescence in maternal blood
The gene encoding human low-molecular weight insulin-like growth-factor binding protein (IGF-BP25): regional localization to 7p12–p13 and description of a DNA polymorphism
Haplotype frequencies of the collagen type-I genes in the Italian population
Impairment of capping in lymphoblastoid cell lines of Duchenne patients indicates an intrinsic cellular defect
Different haplotypes for cystic fibrosis-linked DNA polymorphisms in Polish and Dutch populations
Probe walking: development of novel probes for DNA fingerprinting
Coincident maternal meiotic nondisjunction of chromosomes X and 21 without evidence of autosomal aysnapsis
Molecular and cytogenetic analysis of an interstitial 20p deletion associated with syndromic intrahepatic ductular hypoplasia (Alagille syndrome)
Use of variable simple sequence motifs as genetic markers: application to study of myotonic dystrophy
Human BF*F-subtypes: segregation analysis with inclusion of MHC haplotypes
Sublocalization of von Willebrand factor pseudogene to 22q11.22?q11.23 by in situ hybridization in a 46,X,t(X;22)(pter;q11.21) translocation
Correlation between chromosomal breakpoint positions and synaptic behaviour in human males heterozygous for a pericentric inversion
Chromosome abnormalities in early pregnancy analyzed by direct chromosome preparation of chorionic villi
Assignment of the gene(s) involved in the expression of the proliferation-related Ki-67 antigen to human chromosome 10
Trisomy 18 in monozygotic twins
Deletion 3q27?3qter in an infant with mild dysmorphism, parietal meningocele, and neonatal miliaria rubra-like lesions
Detection of a rare allele with the pMP6d-9/MspI RFLP near the cystic fibrosis locus
In situ hybridization localizes the human putative oncogene GLI to chromosome subbands 12q13.3?14.1
Haplotype analysis of familial amyloidotic polyneuropathy
Differential associative behaviour of mitotic and meiotic acrocentric chromosomes
Mapping of the gene encoding the multifunctional protein carrying out the first three steps of pyrimidine biosynthesis to human chromosome 2
Pseudodeficiency of arylsulfatase A: a common genetic polymorphism with possible disease implications
Chromosomal localization of ARSB, the gene for human N-acetylgalactosamine-4-sulphatase
Four DNA polymorphisms in the LDL-receptor gene and their use in diagnosis of familial hypercholesterolemia
Genetics of the quantitative Lp(a) lipoprotein trait
A new polymorphic marker very closely linked to DXS52 in the q28 region of the human X chromosome
A hereditary double double-banded variation in the vitamin D-binding protein (GC) system analyzed by immunoblotting: duplication of the 1F and 1A2 genes?
Unbalanced translocation between chromosomes 2 and 7 with de novo deletion of band 35 on the long arm of chromosme 2
PLG A91 and PLG M6: two new plasminogen allotypes in Japan
EcoRI RFLP in the human thyroid peroxidase (TPO) gene on chromosome 2
Response to Wiberg's remarks on our article: ?H-Y antigenicity of human fibroblasts?
Molecular characterization of a ring chromosome 14 showing that the PI locus is centromeric to the D14S1 and IGH loci
The human cystatin C gene (CST3), mutated in hereditary cystatin C amyloid angiopathy, is located on chromosome 20
Pregnancy-specific ?1-glycoprotein: cDNA cloning, tissue expression, and species specificity of one member of the PS?G family
Restriction analysis of chromosomal sequences homologous to single-copy fragments cloned from small polydisperse circular DNA (spcDNA)
Dose-response function for Painter's SCE-model
The factor IX BamHI polymorphism: T-to-G transversion at the nucleotide sequence-561
Identification of a common molecular basis for combined 17?-hydroxylase/17,20-lyase deficiency in two Mennonite families Mennonite families
Close linkage of MEN2A with RBP3 locus in Japanese kindreds
Specific amplification of the ZFY gene to screen sex in man
Life tables for Down syndrome
Dicarboxylic aminoaciduria associated with mental retardation
Recurrences of trisomy 18 and trisomy 13 after trisomy 21
Renin locus restriction fragment length polymorphism
Announcements
Diagnosis of genetic disease using recombinant DNA. Second edition
Clinical and biochemical studies in three patients with severe early infantile Cockayne syndrome
Linkage analysis of hereditary thyroid carcinoma with and without pheochromocytoma
Two distinct variants of erythrocyte spectrin ?IV domain
Deletion/frameshift mutation in the ?1 null allele, PI*QObolton
Linkage disequilibrium and CF allele segregation analysis in cystic fibrosis families in Northern Ireland
TaqI polymorphism within the c-Ha-ras-1 VTR is associated with melanoma
Announcements
A new familial syndrome with impaired function of three related peptide growth factors
Linkage studies of the Wiskott-Aldrich syndrome: polymorphisms at TIMP and the X chromosome centromere are informative markers for genetic prediction
Evidence for male X chromosomal mosaicism in X-linked agammaglobulinemia
Genotoxic effect of benzene hexachloride in cultured human lymphocytes
Distribution of meiotic recombination along nondisjunction chromosomes 21 in Down syndrome determined using cytogenetics and RFLP haplotyping
Regional chromosomal assignment of the human glucocorticoid receptor gene to 5q31
X-linked megalocornea: close linkage to DXS87 and DXS94
Expression of the human ETS-2 oncogene in normal fetal tissues and in the brain of a fetus with trisomy 21
Localization of polymorphic DNA probes frequently deleted in lung carcinoma
Heterogeneity of chromosomal breakage levels in epithelial tissue of ataxia-telangiectasia homozygotes and heterozygotes
Linkage disequilibrium for DNA haplotypes near the cystic fibrosis locus in two South European populations South European populations
The human homolog of the myeloproliferative virus maps to chromosome band 1p34
Restriction fragment length polymorphism of human aldehyde dehydrogenase 1 and aldehyde dehydrogenase 2 loci
Population cytogenetics of folate-sensitive fragile sites
Genotypes of alcohol dehydrogenase and aldehyde dehydrogenase loci in Japanese alcohol flushers and nonflushers Japanese
Regional assignment of the loci for adenylate kinase to 9q32 and for ?1-acid glycoprotein to 9q31-q32
Parental age and the origin of trisomy 21
Physical mapping of DXS134 close to the DXS52 locus
Cytogenetic and in situ DNA-hybridization studies in intracranial tumors of a patient with central neurofibromatosis
The absence of type II collagen and changes in proteoglycan structure of hyaline cartilage in a case of Langer-Saldino achondrogenesis
DNA restriction fragment length polymorphisms in differential diagnosis of genetic disease: application in neuromuscular diseases
Non C-banding variants in some normal families might be homogeneously staining regions
The role of recombination in the evolvement of the fragile X mutation
Mapping the human ZFX locus to Xp21.3 by in situ hybridization
Localization of human platelet proteoglycan gene to chromosome 10, band q22.1, by in situ hybridization
Remarks on the article “Use of linkage equilibrium data in prenatal diagnosis of cystic fibrosis” by L. Strain et al.
Preliminary exclusion of an X-linked gene in Leber optic atrophy by linkage analysis
Mitochondrial DNA polymorphism in Finnish families with Leber's hereditary optic neuroretinopathy Finnish
Interaction at clinical level between erythrocyte acid phosphatase and adenosine deaminase genetic polymorphisms
Isolation of a DNA probe of potential use for diagnosis of the fragile-X syndrome
Digoxigenated oligonucleotide probes specific for simple repeats in DNA fingerprinting and hybridization in situ
The gene coding for the p68 calcium-binding protein is localised to bands q32?q34 of human chromosome 5, and to mouse chromosome 11
Molecular cloning of the translocation breakpoint in T-ALL 11;14 (p13;q11): genomic map of TCR alpha and delta region on chromosome 14q11 and long-range map of region 11p13
A rapid method for detection of Y-chromosomal DNA from dried blood specimens by the polymerase chain reaction
Assignment of human aldolase C gene to chromosome 17, region cen?q21.1
Tissue specificity of chromosomal rearrangements in ataxia-telangiectasia
Molecular analysis of the isochromosome 12P in the Pallister-Killian syndrome
Apolipoprotein (apo) E genotypes by polymerase chain reaction and allele-specific oligonucleotide probes: no detectable linkage disequilibrium between apo E and apo CII
The ? subunit locus of the human fibronectin receptor: DNA restriction fragment length polymorphism and linkage mapping studies
Erratum
Molecular defects of type III procollagen in Ehlers-Danlos syndrome type IV
Genetic studies of human apolipoproteins
Cytogenetic studies on three pheochromocytomas derived from patients with von Hippel-Lindau syndrome
Newborn screening by DNA analysis of dried blood spots
Determining informativity of marker typing for genetic counseling in a pedigree
Myotonia congenita (Thomsen's disease) excluded from the region of the myotonic dystrophy locus on chromosome 19
Characterization of a panel of somatic cell hybrids for subregional mapping along 11p and within band 11p13
The levels of ?, ?, and ? chains in patients with Hb H disease
Amplification of satellite III DNA in an unusually large chromosome 14p+ variant
Family study of common fragile sites
Polyclonal hyper-immunoglobulin G1(A1) syndrome
Partial trisomy of distal 8q derived from mother with mosaic 8q23.3?24.13 deletion, and relatively mild expression of trichorhinophalangeal syndrome I
Use of linkage disequilibrium data in prenatal diagnosis of cystic fibrosis
Sister chromatid exchange analysis of the 15q11 region in Prader-Willi syndrome patients
Rejoining between 9q+ and Philadelphia chromosomes results in normal-looking chromosomes 9 and 22 in Ph1-negative chronic myelocytic leukemia
Inheritance of mitochondrial aldehyde dehydrogenase: genotyping in Chinese, Japanese and South Korean families reveals dominance of the mutant allele
Characterization of patients with glycerol kinase deficiency utilizing cDNA probes for the Duchenne muscular dystrophy locus
Familial ring (20) chromosomal mosaicism
Different Hoechst 33342 and DAPI fluorescence of the human Y chromosome in bivariate flow karyotypes
Genetic polymorphism of human peptidase C, PEPC (E.C.3.4.1.1): formal genetic and population data
Reply to letter by Knoll et al.
Non-random aberrant breakpoints in chronic myelogenous leukaemia revisited
Galactose-1-phosphate uridyl transferase in density-fractionated erythrocytes
Radioresistant DNA synthesis and human genetic disease
The aniridia-Wilms' tumour association: molecular and genetic analysis of chromosome deletions on the short arm of chromosome 11
Kinetochore development in two dicentric chromosomes in man
Family and population studies on the human pepsinogen A multigene family
Nucleolar structures in chromosome and SC preparations from human oocytes at first meiotic prophase
Brachytelephalangic chondrodysplasia punctata: a possible X-linked recessive form
Demonstration of spontaneous XX/XY chimerism by DNA fingerprinting
Gm and Km allotypes in 74 Chinese populations: a hypothesis of the origin of the Chinese nation
Mapping studies of the serum cholinesterase-2 locus (CHE2)
Increased frequencies of sister chromatid exchanges at common fragile sites (1)(q42) and (19)(q13)
Epigenetic changes may contribute to the formation and spontaneous regression of retinoblastoma
Chromosomal localization of human aspartate aminotransferase genes by in situ hybridization
DNA haplotypes and frameworks linked to the ?-globin locus in an Austro-Asiatic population with a high prevalence of hemoglobin E Austro-Asiatic population
Regional localization of human ecto-5?nucleotidase to chromosome 6q14?q21
Cytosine methylation and the fate of CpG dinucleotides in vertebrate genomes
RELP-discordance within the human phenylalanine hydroxylase locus
Congenital hyperthyroidism with reciprocal translocation t(1;17)(q25;q21)
On the parental origin of the deletion in Angelman syndrome
Two type II keratin genes are localized on human chromosome 12
A linkage group with FRA16B (the fragile site at 16q22.1)
Centromeric alpha satellite DNA amplification and translocation in an unusually large chromosome 14p+ variant
Increased spindle resistance to antimicrotubule agents in cells prone to chromosomal nondisjunction
An unusual translocation associated with recurrent spontaneous abortions
The problem of our common mitochondrial mother
Disomic homozygosity in 21-trisomic cells: a mechanism responsible for transient myeloproliferative syndrome
Three novel partial deletions of the low-density lipoprotein (LDL) receptor gene in familial hypercholesterolemia
Fragile sites and breakpoints in constitutional rearrangements and in human sperm chromosomes
A case of hereditary persistence of fetal hemoglobin caused by a gene not linked to the β-globin cluster
Mapping the mutation causing the X-linked lymphoproliferative syndrome in relation to restriction fragment length polymorphisms on Xq
Linkage analysis of seven kindreds with the X-linked lymphoproliferative syndrome (XLP) confirms that the XLP locus is near DXS42 and DXS37
Hungarian surveillance of germinal mutations
MASA syndrome: further clinical delineation and chromosomal localisation
The predictive value of chorionic villus histology for identifying chromosomally normal and abnormal spontaneous abortions
Detection of ?-thalassemia and hemoglobin E genes in Thai by a DNA amplification technique
Lack of complementation between xeroderma pigmentosum complementation groups D and H
Frequency and molecular types of deletional α-thalassemia in Egypt
Isolation and characterization of the complete human ?-myosin heavy chain gene
Increase of sister chromatid exchanges in excision repair deficient xeroderma pigmentosum
Regional localization of the TIMP gene on the human X chromosome
Expression of fragile sites in human sperm and lymphocyte chromosomes
Expression of folate-sensitive fragile sites in lymphocyte chromosomes
Analysis of two 47,XXX males reveals X-Y interchange and maternal or paternal nondisjunction
Til 1 ? a human lymphoblastoid cell line with minimal DNA methylation
The human homologues of Fim1, Fim2/c-Fms, and Fim3, three retroviral integration regions involved in mouse myeloblastic leukemias, are respectively located on chromosomes 6p23, 5q33, and 3q27
A Pro → Leu substitution in codon 369 of the alpha-1-antitrypsin deficiency variant PI MHeerlen
Molecular definition of the 11p15.5 region involved in Beckwith-Wiedemann syndrome and probably in predisposition to adrenocortical carcinoma
Chromosomal assignment of two myosin alkali light-chain genes encoding the ventricular/slow skeletal muscle isoform and the atrial/fetal muscle isoform (MYL3, MYL4)
A ?-thalassemia mutant caused by a 300-bp deletion in the human ?-globin gene
Controversy concerning paternal age effect in 47,+21 Down's syndrome
Genetic polymorphism of the apolipoprotein B gene locus influences serum LDL cholesterol level in familial hypercholesterolemia
Apolipoprotein B amino acid 3611 substitution from arginine to glutamine creates the Ag (h/i) epitope: the polymorphism is not associated with differences in serum cholesterol and apolipoprotein B lev
Maternal origin of a de novo chromosome 8 deletion in a patient with Langer-Giedion syndrome
Chromosomal localization of human glutathione transferase genes of classes alpha, mu and pi
Chromosomal characteristics of malignant lymphoma
The gene for human interleukin 7 (IL7) is at 8q12-13
Is there a correlation between morphological and cytogenetic findings in placental tissue from early missed abortions?
Inactivated X chromosome fold in human leukemia and related clonal disorders
Tissue-specific 45,X0/47,XY,+13 mosaicism in an 18-year-old woman
A new polymorphic variant of human complement factor I
Gene symbols for fragile sites: a proposal
Study of restriction fragment length polymorphisms at the human phenylalamine hydroxylase locus and evaluation of its potential application in prenatal diagnosis of phenylketonuria in Chinese Chinese
Linkage analysis of the Duffy blood group marker with several chromosome 1 genes in an extended pedigree with Charcot-Marie-Tooth disease
Incontinentia pigmenti and X-autosome translocations
Linkage of X-linked retinitis pigmentosa to the hypervariable DNA marker M27? (DXS255)
Demonstration of a Sandhoff disease-associated autosomal 50-kb deletion by field inversion gel electrophoresis
Nucleolus organizer regions (NORs) inserted in 6q15
Duplication of an Xp segment that includes the ZFX locus causes sex inversion in man
Genetic polymorphism of human urine deoxyribonuclease I
Remarks on the article ?H-Y antigenicity of human fibroblasts? by C. Jorgensen and E.J. Eichwald
Announcements
Increased detectability of somatic changes in the DNA from human tumours after probing with ?synthetic? and ?genome-derived? hypervariable multilocus probes
Prenatal enzymatic diagnosis of Krabbe disease (globoid-cell leukodystrophy) using chorionic villi
Why is the cystic fibrosis gene so frequent?
Linkage of PGK1 to X-linked severe combined immunodeficiency (IMD4) allows predictive testing in families with no surviving male
G2 chromosomal radiosensitivity in families with ataxia-telangiectasia
Close linkage of probe p212 (DXS178) to X-linked agammaglobulinemia
Physical fine-mapping of a deletion spanning the Norrie gene
The volumes and morphology of human chromosomes in mitotic reconstructions
Cytogenetic and molecular analysis of an unbalanced translocation (X;7) (q28;p15) in a dysmorphic girl
Molecular characterisation of three alpha-1-antitrypsin deficiency variants: proteinase inhibitor (Pi) nullcardiff (Asp256?Val); Pi Mmalton (Phe51? deletion) and Pi I (Arg39?Cys)
The gene encoding the human preproacrosin (ACR) maps to the q13-qter region on chromosome 22
Isochromosome not translocation in trisomy 21q21q
Haplotype and multipoint linkage analysis in Finnish choroideremia families
A search for restriction fragment length polymorphism on the human Y chromosome
Human interferon gamma receptor 1 (IFNGR1) gene maps to chromosome region 6q23–6q24
Phenylketonuria: detection of a frequent haplotype 4 allele mutation
Unusual chromosome 20 anomaly arising ?de novo? to give dic(20)qs
Reply to letter by J. H. Robbins
Three F XIIIA gene loci?
Fragile sites and statistics
Editorial help
Announcements
Localization of the active type I DNA topoisomerase gene on human chromosome 20q11.2-13.1, and two pseudogenes on chromosomes 1q23-24 and 22q11.2-13.1
Molecular basis of ?-thalassemia in Thailand: analysis of ?-thalassemia mutations using the polymerase chain reaction
The spectrum of ?-thalassemia mutations in northern and northeastern Thailand
Cell type-dependent difference in the distribution and frequency of aphidicolin-induced fragile sites: T and B lymphocytes and bone marrow cells
DNA Fingerprinting with the oligonucleotide probe (CAC)5/(GTG)5: somatic stability and germline mutations
Gene assignment of Zellweger syndrome to 7q11.23: report of the second case associated with a pericentric inversion of chromosome 7
Rate of chromosomal aberrations in prenatally detected hydrops fetalis and hygroma colli
Use of transgenic mice for the characterization of human alpha 1-acid glycoprotein (orosomucoid) variants
No lack of complementation for unscheduled DNA synthesis between xeroderma pigmentosum complementation groups D and H
Reply to letter by M. De Braekeleer