Clinical Genetics - 1972

64 articles | Last updated: 2025-12-03 14:12:56
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Article Title Cauc. White Euro. Other Phrases Used
T A T A T A T A
David Y.‐Y. Hsia … In Memoriam
Low dopamine‐β‐hydroxylase activity in Down's syndrome
Chondrodystrophia calcificans congenita (Conradi's disease) in a mother and her child
The XYY syndrome in an adolescent male exhibiting prominent behavioral problems
Giemsa banding patterns of human chromosomes*
Studies on inherited antigenic variati on of human serum ß‐lipoprotein by passive hemagglutination
ABO blood groups, serum cholesteryl esters and plasma lecithin: cholesterol acyltransferase activity
Studies on the protein moiety of serum high density lipoprotein from patients with familial lecithin: cholesterol acyltransferase deficiency
Studies on inherited antigenic variation of human serum β‐lipoprotein by passive hemagglutination
The syndrome of ectrodactyly, ectodermal dysplasia and cleft lip and palate: report of a family demonstrating a dominant inheritance pattern
The Rubinstein‐Taybi syndrome. Report of 7 cases
Group‐specific component and haptoglobin distributions in schizophrenic states racial background
Haptoglobin distributions in Down's syndrome Mongoloid
Erythrocyte acid phosphatase distributions in normal, schizophrenic and mentally retarded subjects
A differential staining technique for chromosome identification and its comparison with fluorescence technique
Down's syndrome in twins
A marker algebra
Localization of male determining factor on short arm of Y chromosome Case report of a baby with 46, x, t (Yp+;14q‐)
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
Ectrodactyly‐ectodermal dysplasia‐clefting (EEC) syndrome
Presence of ß‐lipoprotein in serum of patients treated for acrodermatitis enteropathica (Danbolt's disease)
Correlation between colour vision disturbance and appetite for alcohol
Juvenile GM<sub>1</sub> gangliosidosis: Clinical, pathological, chemical and enzymatic studies
Pseudo‐achondrogenesis with fractures
Dentinogenesis imperfecta: severe expression in a probable homozygote
Australia antigen and Down's syndrome
Variability in mongolism ‐a comparison of the hand skeleton in mongoloids and normals
Attempted detection of heterozygotes for maple‐syrup‐urine disease
Rheumatoid arthritis in the 46, XX, 18p‐ syndrome
8‐trisomy in the bone marrow. Report of two cases
Effects of the XYY karyotype in one of two brothers with congenital adrenal hyperplasia
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
PEDIG ‐ A computer program for calculation of genotype probabilities using phenotype information
Pseudovaginal perineoscrotal hypospadias
A case of classical maple syrup urine disease “Thiamine non‐responsive”
Induction of testis alcohol dehydrogenase in prepubertal rats
Pure gonadal dysgenesis
Brachydactyly type A<sub>2</sub> in an American Negro family American Negro family
Hypophosphatasia: screening and family investigations in an endogamous Hungarian village
Evolution of palmar skin creases in the Ehlers‐Danlos syndrome
DNA synthesis of human XYY cells
Unusual features in familial asphyxiating thoracic dysplasia (Jeune's disease) Greek origin; Arabic and Greek origin
Polymorphism of the human Y chromosome: Fluorescence microscopic studies on the sites of morphologic variation
High frequency of atypical pseudocholinesterase gene among Iraqi and Iranian Jews* European Jews; Iraqi and Iranian Jews; non-Ashkenazi Jews from Iraq, Yemen and North Africa; North African Jews
Familial polysyndactyly and craniofacial anomalies
Three non‐mongoloid patients of similar phenotype with an extra G‐like chromosome
The effects of genetic counselling in Duchenne muscular dystrophy
A chromosome survey of a hospital for the mentally subnormal Part 1: Sex chromosome abnormalities
Chromosome survey of a hospital for the mentally subnormal Part 2: Autosome abnormalities
A ring chromosome (No. 18) in a cyclops
Genetic studies in a family with testicular feminization, haemophilia A and colour blindness
X‐linked mental retardation and/or hydrocephalus
Identification of 21 r and 22r chromosomes by quinacrine fluorescence antimongolism
Familial occurrence of mild hyperlipoproteinaemias
Length of the Y chromosome in criminal males
Possibility of culturing foetal cells at early stages of pregnancy
Dyschondrosteosis. A Mexican family with two affected males
A quantitative method for determining γG allotype antigens Chinese; Easter Islanders; different ethnic groups
Thyroid antibodies: A study of first degree relatives
Cytogenetic findings in a parent of a patient with Fanconi's anemia
The relation of some features of Huntington's disease to the age at onset of symptoms in parents
Zymograms of the human red cell acid phosphatase obtained with different substrates
The ectrodactyly‐ectodermal dysplasia‐clefting (EEC) syndrome
Problems in prenatal diagnosis resulting from chromosomal mosaicism