The genetic basis for the variabilityof hereditable diseases
- 1 May 1968
- journal article
- research article
- Published by Elsevier in The Journal of Pediatrics
- Vol. 72 (5), 727-736
- https://doi.org/10.1016/s0022-3476(68)80023-x
Abstract
No abstract availableThis publication has 19 references indexed in Scilit:
- Genetic and clinical heterogeneity in the oral-facial-digital syndromesThe Journal of Pediatrics, 1967
- CELLULAR METACHROMASIA, A GENETIC MARKER FOR STUDYING THE MUCOPOLYSACCHARIDOSESThe Lancet, 1967
- Negro Variant of Glucose-6-Phosphate Dehydrogenase Deficiency (A - ) in ManScience, 1967
- Dysmorphology (teratology)The Journal of Pediatrics, 1966
- Heterozygotes for cystinuriaAnnals of Human Genetics, 1966
- ADENOSINE-TRIPHOSPHATASE DEFICIENCY IN PATIENTS WITH NON-SPHEROCYTIC HEMOLYTIC ANÆMIAThe Lancet, 1964
- Studies in Congenital Non-Spherocytic Haemolytic Anaemias with Specific Enzyme DefectsActa Haematologica, 1964
- Evidence for Non-Allelism between Genes Affecting Human Serum CholinesteraseNature, 1963
- Hereditary Absence of Reduced Glutathione in the Erythrocytes — a New Clinical and Biochemical Entity?Vox Sanguinis, 1961
- PHENOTYPES AND GENOTYPES IN CYSTINURIAAnnals of Human Genetics, 1955