| Fetal mortality in oral cleft families (VI): A search for early embryonic and zygotic mortality |
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| Gonadoblastoma in a patient with an isodicentric X chromosome |
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| Incidence of classic PKU in Italy estimated from consanguineous marriages and from neonatal |
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| Facial weakness and oligosyndactyly: ? independent variable features of familial type of the Möbius syndrome |
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| X‐linked mental retardation, growth retardation, deafness and micro‐genitalism. A second familial report |
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| Do the MN and Jk systems influence environmental variability in serum lipid levels? |
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| The epidemiology of conjoined twinning in Southern Africa |
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| Familial cancer or cancer family syndrome. Report on a cancer family and consideration of genetic mechanisms |
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| Dermoodontodysplasia: an eleven‐member, four generation pedigree with an apparently hitherto undescribed pure ectodermal dysplasia |
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| A Rothmund‐Thomson case with hypertension |
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| 45 XO/49 XYYYY Mosaicism in a male with stigmata of Turner's syndrome |
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| Letter to the Editors |
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| Autosomal dominant craniometaphyseal dysphasia. Clinical variability |
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| <i>In vitro</i> growth characteristics of skin fibroblasts from patients with adenomat‐osis of the colon and rectum and their reIatives |
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| Correlation between testicular tissue and H‐Y phenotype in intersex patients |
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| Catechol‐O‐methyltransferase activity in erythrocytes and plasma dopamine‐B‐hydroxylase activity in familial Minimal Brain Dysfunction |
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| Reproductive drive and genetic counselling |
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| Two different structural abnormalities of chromosome 13 in offspring of chromo‐somally normal parents with two fragile sites |
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| An azoospermic male with presumably balanced reciprocal translocation |
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| HLA A antigens in HLA 627 positive acute anterior uveitis |
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| Natural history of the organic acidurias? A call for information |
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| A study of mental retardation in children in the Island of Hawaii |
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| Infantile lethal neuraminidase deficiency (sialidosis) |
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| Myotonic dystrophy: limited electromyo‐graphic abnormalities in 2 definite cases |
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| Clinical heterogeneity in a sibship with Niemann‐Pick disease type C |
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| Genetic aspects of artificial insemination by donor (AID). Indications, surveillance and results |
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| Karyotype 47, XXY,18p‐ in a newborn child with holoprosencephaly |
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| Chronic granulomatous disease carrier geno‐dermatosis (CGDCGD) |
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| Family resemblance for fasting blood glucose in a population of Japanese Americans |
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Japanese |
| The fragile X chromosome in a large Indian kindred |
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✓ |
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Indian; ethnic groups |
| Reflections on muscular dystrophy in a Sudanese kindred |
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| Letters to the Editors |
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| Announcements |
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| Erratum |
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| Comparative diagnostic value of phenyla‐lanine challenge and phenylalanine hydroxylase activity in phenylketonuria |
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| Blood pressure and myotonic dystrophy |
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| Xeroderma Pigmentosum Registry |
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| Cytogentic studies of a patient with mosaicism of isochromosome 13q and a dicentric (Y; 13) translocation showing differential centromeric activity |
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| Famillial pericentric inversion of chromosome 9, INV (9)(p22q32) with recurrent duplication‐deletion |
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| A New Solution to Procreation |
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| Family distances can reveal hidden consanguinity |
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✓ |
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Western European societies |
| Sphingomyelinase in cultured skin fibroblasts from normal and Niemann‐Pick type C patients |
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| Chromosome preparations of human whole blood lymphocytes: an improved technique |
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| Greig cephalopolysyndactyly: report of 13 affected individuals in three families |
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| An unusual otological manifestation of Usher's syndrome in four siblings |
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| Letter to the Editors |
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| Trisomy 4p in four relatives: variability and lack of distinctive features in phenotypic expression |
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| Cystic hygroma and hydrops fetalis in a fetus with trisomy 13 |
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| Fragile X syndrome in mildly mentally retarded children in a Northern Swedish county. A prevalence study |
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| Genetic regulation of melatonin excretion in urine |
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| Male to male transmission of the G syndrome |
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| Silver‐Russell syndrome with absence of digits and syndactylism of the fingers |
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| Spongy degeneration of the brain in Israel: A retrospective study |
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Ashkenazi; Sephardi; Oriental; Jewish |
| Homology between coding and noncoding sequences within the human class I HLA antigen gene |
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| Recessive gonadal dysgenesis |
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| X‐chromosome polysomy in the female: personal experience and review of the literature |
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| Autosomal dominant inheritance of conductive deafness due to stapedial anomalies, external ear malformations and congenital facial palsy |
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Indian stock |
| Inherited 13/14 translocation and meta‐centric microchromosome associated with trisomy 21: Report of 2 cases |
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| The First International Symposium on Reproductive Medicine |
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| Monosomy 21 syndrome: Further delineation including clinical, neuropathological, cytogenetic and biochemical studies |
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| Sister chromatid exchange and lym phocyte proliferation in a Down syndrome mosaic |
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| Δ‐Aminolevulinatedehydrase: synteny with ABO‐AK1‐ORM (and assignment to chromosome 9) |
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| ABSTRACTS |
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| HLA and disease: Haplotype sharing in multiplex families |
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| Translocations in Prader‐WiIIi syndrome |
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| Tandem duplication of chromosome 14 (q24+q32) in male newborn with congenital malformations |
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| A new syndrome of short stature, joint limitation and muscle hypertrophy |
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| Folic acid metabolism in patient with fragile X |
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| An HLA‐All Assoiciation with the hemochromatosis allele? |
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| Replication and inactivation of and isodicentric X: presence of an inactive centromere influences the replication patterns |
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| Dominant ano‐rectal malfromatin, nephritis and nerve‐deafness: a possible new entity? |
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| Frontonasal dysplasia, coronal cranisoynostosis, pre‐ and postaxial polydactyly and split nails: a new autosomal dominant mutant with reduced penetrance and varibale expression? |
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| A new from of residual hexosaminidase activity in infantile Tay Sachs disease fibroblasts |
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| A further case of monosomy 10qter |
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| Lymphocyte proliferation in a 31‐week premature neonate with 69, XXX chromosomal constitution* |
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| The Mohr syndrome: are there two variants? |
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| LETTERS TO THE EDITORS |
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| Announcements |
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| Congenital adrenal hypoplasia, progressive muscular dystrophy, and severe mental retardation, in association with glycerol kinase deficiency, in male sibs |
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| Announcements |
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| European Society of Human Genetics Abstracts from Symposium on “Autosomal Heterozygosity” |
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| Partial trisomy 16q in two boys resulting from a maternal translocation, t(15;16) (p12;q11) |
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| Y chromosome length related to fetal loss |
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| The Aarskog syndrome in a large family, suggestive for autosomal dominant inheritance |
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| Prader‐Willi syndrome associated with inversion of chromosome 15 |
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| Formal analysis of dysmorphism: Objective methods of syndrome definition |
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| Glycinelserine ratios in amniotic fluid: an unreliable indicator for the prenatal diagnosis of nonketotic hyperglycinemia |
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| A lethal neonatal variant of carbamoyl‐phosphate synthetase deficiency in combination with an intermediate activity of L‐ornithine: 2‐oxoglutarate amino‐transferase |
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| Fetal ABO blood group typing using amniotic fluid |
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| Heterogeneity in mucolipidosis II (l‐cell disease) |
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| Fetoscopic photography |
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| Interstitial deletion in the long arm of chromosome no. 5 |
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| A linkage study of the HLA region using C‐band heteromorphisms |
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| Partial trisomy 2q |
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| Author Index |
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| Detection of Fabry's disease heterozy. gotes by enzyme analysis in single fibroblasts after cell sorting |
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| Silent microcephaly: A distinct autosomal dominant trait |
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| Cytogenetics of recurrent abortions |
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| Diagnosis of cystic fibrosis homozygotes and heterozygotes from plasma and fibroblast cultures. A three‐generation family study |
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| Four brothers with mental retardation, spastic paraplegia and palmoplantar hyperkeratosis. A new syndrome? |
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✓ |
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| Letters to the Editors |
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| Marker X‐associated mental retardation A study of 150 retarded males |
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| Aspartylglucosaminuria in the United States |
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✓ |
✓ |
Finnish populations; (also appears as 'nowFinnish' in the abstract, likely a typo for 'non-Finnish') |
| The Sixth Annual New York March of Dimes Symposium on Genetics for the Practicing Physician |
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| Germinal mosaicism in achondroplasia: a family with 3 affected siblings of normal parents |
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| Gentics and linkage relationships of the C3 polymorphism: discovery of C3‐Se linkage and assignment of LES‐C3‐DM‐Se‐PEPD‐Lu synteny to chromosome 19 |
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| The half chromatid mutation model and bidrectional mutation in incontinentia pigmenti |
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| Is there a predisposition for meiotic non‐disjunciton that may be detected by mitoitc hyperploidy? |
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| Fetal mortality in oral cleft families(IV): the “doubling effect” |
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✓ |
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several different backgrounds of European ancestry |
| Oromandibular limb hypogenesis/Hanhart's syndrome: possible drug influence on the malformation |
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| Trisomy 10p produced by recombination involving complex paternal translocation between chromosomes 1 and 10 |
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| Chromosome aneuploidy in Alzheimer's disease |
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| Partial trisomies 15 |
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| Characterization of a Y/15 translocation by banding methods, distamycin A treatment of lymphocytes and DNA restriction endonuclease analysis |
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| Aberrant twinning (diprosopus) associated with anencephaly |
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| Two cases of prenatal diagnosis of a satellited Yq chromosome |
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| A familial X/Y translocation in a boy with ichthyosis, hypogonadism and mental retardation |
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| Genetic regulation of the red cell uroporphyrinogen‐l‐synthetase level in families with acute intermittent porphyria |
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| Additional data on spontaneous abortion and facial cleft malformations |
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| Association between the degree of mosaicism and the severity of syndrome in Turner mosaics and Klinefelter mosaics |
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| The relevance of pre‐amniocentesis pedigree analysis and genetic counseling |
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| Linkage analysis in von Willebrand disease |
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| The femur, fibula, ulna (FFU) complex in siblings |
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| The hypertelorism—hypospadias syndrome |
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| High resolution chromosome banding in the Rubinstein—Taybi syndrome |
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| Fetal mortality and cleft lip with or without cleft palate |
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| Polycystic disease of liver: an entity of its own or not? |
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| Fetal mortality in oral cleft families: data from Indiana and Montreal |
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| Biochemical abnormalities in connective tissue of osteodysplasty of Melnick‐Needles and dyssegmental dwarfism |
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| A simplified PKU gene carrier detection test using fasting blood |
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| Chromosomal breakage in multiple endocrine adenomatosis (types I and II) |
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| Mixed gonadal dysgenesis and sex chromosome mosaicism with multiple cell lines including structural aberrations of the Y chromosome |
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| The wrinkly skin syndrome: A report of two siblings from Saudi Arabia |
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| The Rubinstein‐Taybi syndrome: Occurrence in two sets of identical twins |
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| Population genetic analyses of insulin dependent diabetes mellitus using HLA allele frequencies |
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| The strength of association between fragile(X) chromosome presence and mental retardation |
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| Turner syndrome patients with a ring X chromosome |
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| Letter to the Editors |
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