| Editorial |
|
|
|
|
|
|
|
|
|
| Use of white blood cells and cultured somatic cells in clinical genetic disorders |
|
|
|
|
|
|
|
|
|
| Abnormalities of human sex chromosomes. V. A unifying concept in relation to the gonadal dysgeneses |
|
|
|
|
|
|
|
|
|
| A new ceruloplasmin variant, Cp Galveston |
|
|
|
|
|
|
|
|
|
| Sex difference in alcohol metabolism; androgenic steroid as an inducer of kidney alcohol dehydrogenase |
|
|
|
|
|
|
|
|
|
| Lmmunobiology of human anti‐lgA: a serologic and immunogenetic study of immunization to IgA in transfusion and pregnancy* |
|
✓ |
|
|
|
|
|
|
|
| Gardner's syndrome: Formal genetics and statistical analysis of a large Canadian kindred |
|
|
|
|
|
|
|
|
|
| Discontinuity and quasi‐continuity: Alternative hypotheses of multifactorial inheritance |
|
|
|
|
|
|
|
|
|
| A pedigree with essential myoclonus and genetic spastic oligophrenia* |
|
|
|
|
|
|
|
|
|
| Antibodies to inherited &‐lipoprotein antigens in the serum of multiply transfused patients |
|
|
|
|
|
|
|
|
|
| Cellular metachromasia in Pompe's disease and Pelizaeus‐Merzbacher disease |
|
|
|
|
|
|
|
|
|
| X‐Linked testicular feminization in the mouse as a non‐inducible regulatory mutation of the Jacob‐Monod type |
|
|
|
|
|
|
|
|
|
| Studies on the genetic polymorphism of the C'3 of human serum |
|
|
|
|
|
|
✓ |
✓ |
Norwegian |
| FamiIial ano‐rectal anornaIy |
|
|
|
|
|
|
|
|
|
| A new method of length analysis of the B group of chromosomes with special reference to the “cri‐du‐chat” syndrome |
|
|
|
|
|
|
|
|
|
| Studies of human chromosomes by DNA-binding fluorochromes I. The normal chromosome complement |
|
|
|
|
|
|
|
|
|
| Further studies on serum α1 lipoprotein in famiIiaI lecithin:cholesteroI acyltransferase deficiency |
|
|
|
|
|
|
|
|
|
| Recessive, sex-Iinked, progressive, oculocerebral degeneration |
|
|
|
|
|
|
|
|
|
| Studies of human chromosomes by DNA‐binding fluorochromes I. The normal chromosome complement |
|
|
|
|
|
|
|
|
|
| Recessive, sex‐I inked, progressive, oculocerebral degeneration |
|
|
|
|
|
|
|
|
|
| Some fine structural and functional features of lymphocytes in “acquired” agammaglobulinernia A genetically determined disease |
|
|
|
|
|
|
|
|
|
| Serum lipoproteins in plasma lecithin:cholesterol acyltransferase deficiency, studied by electron microscopy |
|
|
|
|
|
|
|
|
|
| Precipitating factors against chicken proteins in patients with Down's syndrome |
|
|
|
|
|
|
|
|
|
| Interaction between antilymphocyte globulin and phytohemagglutinin in human lymphocyte cultures |
|
|
|
|
|
|
|
|
|
| Quantitative variation in serum ceruloplasmin among ethnic groups |
|
✓ |
|
|
|
|
✓ |
✓ |
Negroes; Orientals; Amerindians |
| Prevention of rhesus isoimmunization |
|
|
|
|
|
|
|
|
|
| X‐linked cerebellar ataxia |
|
|
|
|
|
|
|
|
|
| Phacomatoses, the inheritance of cancer, and somatic mutation |
|
|
|
|
|
|
|
|
|
| Do the 48, XXYY males have a characteristic phenotype? A Review |
|
|
|
|
|
|
|
|
|
| Red cell acid phosphatase, phenolphthalein diphosphate, and ß-naphtyl phosphate: variation in substrate specificity |
|
|
|
|
|
|
|
|
|
| An X-linked recessive variety of ichthyosis vulgaris different from the X-linked ichthyosis of Wells and Kerr |
|
|
|
|
|
|
|
|
|
| Amino acid composition of the serum low density lipoprotein in pactients with familial lecithin:cholesterol acyltransferase deficiency |
|
|
|
|
|
|
|
|
|
| The 4th International Congress of Human Genetics |
|
|
|
|
|
|
|
|
|
| Phacomatoses, the inheritance of cancer, and somatic mutation |
|
|
|
|
|
|
|
|
|
| Hereditary dystonia musculorum deformans |
|
|
|
|
|
|
|
|
|
| Do the 48, XXYY males have a characteristic phenotype? A Review |
|
|
|
|
|
|
|
|
|
| Red cell acid phosphatase, phenolphthaleindiphosphate, and β‐naphtyl phosphate: variation in substrate specificity |
|
|
|
|
|
|
|
|
|
| Further studies on serum <i>α</i><sub>1</sub>‐lipoprotein in familial lecithin:cholesterol acyltransferase deficiency |
|
|
|
|
|
|
|
|
|
| G E N EX ‐ An algebraic approach to pedigree probability calculus |
|
|
|
|
|
|
|
|
|
| Amino acid composition of the serum low density lipoprotein in patients with familial lecithin<sub>:</sub>cholesterol acyltransferase deficiency |
|
|
|
|
|
|
|
|
|
| Rivanol treatment of cystic fibrosis serum: effect of supernatant upon ciliary action |
|
|
|
|
|
|
|
|
|
| Lesch‐Nyhan syndrome: Rapid detection of heterozygotes |
|
|
|
|
|
|
|
|
|
| Nonrandomness of D‐group chromosomes involved in centric‐fusion translocation |
|
|
|
|
|
|
|
|
|
| Hereditary dystonia musculorum deformans |
|
|
|
|
|
|
|
|
|
| GEN EX- An algebraic approach to pedigree probability calculus |
|
|
|
|
|
|
|
|
|
| An X‐linked recessive variety of ichthyosis vulgaris different from the X‐linked ichthyosis of Wells and Kerr |
|
|
|
|
|
|
✓ |
✓ |
North German kindred |