| David Y.‐Y. Hsia … In Memoriam |
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| Low dopamine‐β‐hydroxylase activity in Down's syndrome |
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| Chondrodystrophia calcificans congenita (Conradi's disease) in a mother and her child |
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| The XYY syndrome in an adolescent male exhibiting prominent behavioral problems |
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| Giemsa banding patterns of human chromosomes* |
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| Studies on inherited antigenic variati on of human serum ß‐lipoprotein by passive hemagglutination |
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| ABO blood groups, serum cholesteryl esters and plasma lecithin: cholesterol acyltransferase activity |
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| Studies on the protein moiety of serum high density lipoprotein from patients with familial lecithin: cholesterol acyltransferase deficiency |
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| Studies on inherited antigenic variation of human serum β‐lipoprotein by passive hemagglutination |
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| The syndrome of ectrodactyly, ectodermal dysplasia and cleft lip and palate: report of a family demonstrating a dominant inheritance pattern |
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| The Rubinstein‐Taybi syndrome. Report of 7 cases |
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| Group‐specific component and haptoglobin distributions in schizophrenic states |
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racial background |
| Haptoglobin distributions in Down's syndrome |
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Mongoloid |
| Erythrocyte acid phosphatase distributions in normal, schizophrenic and mentally retarded subjects |
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| A differential staining technique for chromosome identification and its comparison with fluorescence technique |
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| Down's syndrome in twins |
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| A marker algebra |
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| Localization of male determining factor on short arm of Y chromosome Case report of a baby with 46, x, t (Yp+;14q‐) |
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| An abnormal large human chromosome identified as an end‐to‐end fusion of two X's by combined results of the new banding techniques and microdensitometry |
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| Ectrodactyly‐ectodermal dysplasia‐clefting (EEC) syndrome |
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| Presence of ß‐lipoprotein in serum of patients treated for acrodermatitis enteropathica (Danbolt's disease) |
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| Correlation between colour vision disturbance and appetite for alcohol |
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| Juvenile GM<sub>1</sub> gangliosidosis: Clinical, pathological, chemical and enzymatic studies |
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| Pseudo‐achondrogenesis with fractures |
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| Dentinogenesis imperfecta: severe expression in a probable homozygote |
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| Australia antigen and Down's syndrome |
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| Variability in mongolism ‐a comparison of the hand skeleton in mongoloids and normals |
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| Attempted detection of heterozygotes for maple‐syrup‐urine disease |
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| Rheumatoid arthritis in the 46, XX, 18p‐ syndrome |
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| 8‐trisomy in the bone marrow. Report of two cases |
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| Effects of the XYY karyotype in one of two brothers with congenital adrenal hyperplasia |
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| Some observations on the blood levels of phenylalanine in dilute mice and a comparison between human phenylketonuria and the disease of mice homozygous for the dilute lethal gene |
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| PEDIG ‐ A computer program for calculation of genotype probabilities using phenotype information |
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| Pseudovaginal perineoscrotal hypospadias |
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| A case of classical maple syrup urine disease “Thiamine non‐responsive” |
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| Induction of testis alcohol dehydrogenase in prepubertal rats |
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| Pure gonadal dysgenesis |
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| Brachydactyly type A<sub>2</sub> in an American Negro family |
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American Negro family |
| Hypophosphatasia: screening and family investigations in an endogamous Hungarian village |
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| Evolution of palmar skin creases in the Ehlers‐Danlos syndrome |
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| DNA synthesis of human XYY cells |
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| Unusual features in familial asphyxiating thoracic dysplasia (Jeune's disease) |
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Greek origin; Arabic and Greek origin |
| Polymorphism of the human Y chromosome: Fluorescence microscopic studies on the sites of morphologic variation |
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| High frequency of atypical pseudocholinesterase gene among Iraqi and Iranian Jews* |
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European Jews; Iraqi and Iranian Jews; non-Ashkenazi Jews from Iraq, Yemen and North Africa; North African Jews |
| Familial polysyndactyly and craniofacial anomalies |
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| Three non‐mongoloid patients of similar phenotype with an extra G‐like chromosome |
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| The effects of genetic counselling in Duchenne muscular dystrophy |
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| A chromosome survey of a hospital for the mentally subnormal Part 1: Sex chromosome abnormalities |
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| Chromosome survey of a hospital for the mentally subnormal Part 2: Autosome abnormalities |
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| A ring chromosome (No. 18) in a cyclops |
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| Genetic studies in a family with testicular feminization, haemophilia A and colour blindness |
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| X‐linked mental retardation and/or hydrocephalus |
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| Identification of 21 r and 22r chromosomes by quinacrine fluorescence |
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antimongolism |
| Familial occurrence of mild hyperlipoproteinaemias |
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| Length of the Y chromosome in criminal males |
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| Possibility of culturing foetal cells at early stages of pregnancy |
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| Dyschondrosteosis. A Mexican family with two affected males |
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| A quantitative method for determining γG allotype antigens |
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Chinese; Easter Islanders; different ethnic groups |
| Thyroid antibodies: A study of first degree relatives |
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| Cytogenetic findings in a parent of a patient with Fanconi's anemia |
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| The relation of some features of Huntington's disease to the age at onset of symptoms in parents |
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| Zymograms of the human red cell acid phosphatase obtained with different substrates |
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| The ectrodactyly‐ectodermal dysplasia‐clefting (EEC) syndrome |
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| Problems in prenatal diagnosis resulting from chromosomal mosaicism |
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