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Clinical Genetics - 1971

54 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
Unilateral colour vision disturbance. A family study
Human mitotic and meiotic chromosome damage following in vivo exposure to methotrexate
Hypotonic KCl: An improved method of processing human testicular tissue for meiotic chromosomes
Amino acid naphthylamidase isozymes in cancer cells and normal cells
Biochemical and immunological characterization of ceruloplasmin genetic variants ✓ ✓ Negroes
Meiosis and spermatogenesis in two postpuberal males with Down's syndrome: 47, XY, G+ ✓ ✓ mongoloid
Achondroplasia and thanatophoric dwarfism in the newborn
Male and female sex determination in hair roots
Dominant mode of inheritance in atrial septal defect
Autosomal dominant inheritance in Larsen's syndrome
Amino acid composition of serum high density lipoprotein in patients with familial lecithin:cholesterol acyltransferase deficiency
The adducted thumbs syndrome ✓ ✓ Amish
Cleidocranial dysostosis
Congenitally malformed female infant with hairy pinnae
Studies on inherited antigenic variation of human serum ß‐lipoprotein by passive hemagglutination
Accumulation of different congenital heart defects in one pedigree
The ENCU scoring system
Evidence for autosomal recessive inheritance of costovertebral dysplasia
Glucose‐6‐phosphate dehydrogenase polymorphism: A valuable tool to study tumor origin ✓ ✓ Negro
Studies of human chromosomes by DNA‐binding fluorochromes
Congenital chloride diarrhea, an autosomal recessive disease
Similarity in amino acid composition between human serum lipoproteins and histocompatibility antigens on cell membranes
Spinal muscular atrophy type II
Investigations on the nature of ceruloplasmin deficiency in the newborn
Pre‐beta‐lipoproteins in healthy persons
Choroideremia and the Xg locus: Another look for linkage
Demonstration of an atypical pre‐ ß‐lipoprotein in human serum
See‐saw winking in a familial oral‐facial‐digital syndrome
Heart malformations in two brothers with identical chromosome aberrations (46, XY, G‐ ? F+)
The relation of type of initial symptoms and line of transmission to ages at onset and death in Huntington's disease
Another variant in the C 3 system
Discriminating between different modes of inheritance in genetic disease
Month of birth and gametopathy
Genetics of hereditary nephropathy with deafness (Alport's disease)
Chromosome studies on male patients at a mental subnormality hospital
Serum intestinal alkaline phosphatase, ABO blood group, secretor status, and lipaemia
Large human Y chromosome with two fluorescent bands
Inheritance of Gm(g) and a gene complex <i>Gm</i><sup>a</sup><i>Gm</i><sup>g weak</sup> ✓ ✓ Norwegian families
Identification of D group chromosomes by autoradiography and fluorescence microscopy
Identification of human G–group and Y chromosomes. Demonstration of constitutive heterochromatin by modified DNA/RNA hybridization technique
Sex determination and gonadal differentiation in man
Hereditary enamel hypoplasia
A familial Y/autosome translocation in man
Hypoplastic left heart syndrome: An autosomal recessive disorder
Studies of human chromosomes by DNA‐binding fluorochromes
Clinical applications of polymorphism in chromosome fluorescence
More about X‐linked testicular feminization of the mouse as a noninducible (i<sup>s</sup>) mutation of a regulatory locus: 5α‐androstan‐3α‐17ß‐diol as the true inducer of kidney alcohol dehydrogenase
Incidence of cleft lip and palate in the offspring of cleft parents
Evaluation of dermal patterns in Down's syndrome by predictive discrimination
Familial de Lange syndrome
6‐Phosphogluconate dehydrogenase (6‐P‐GD) in Down's syndrome
Lysinuric protein intolerance, an autosomal recessive disease ✓ ✓ Finnish (phrases: 'diagnosed in 16 patients of 10 families in Finland', 'one Finnish immigrant in Sw
Syndrome characterized by lingual malformation, Polydactyly, tachypnea, and psychomotor retardation (Mohr syndrome)
A genetic and statistical study of some sex‐related factors in Huntington's disease