Linkage Studies in Lenz Microphthalmia
- 1 January 1975
- journal article
- research article
- Published by S. Karger AG in Human Heredity
- Vol. 25 (6), 493-500
- https://doi.org/10.1159/000152765
Abstract
Glucose-6-phosphate dehydrogenase (G6PD) phenotype studies were done on a black family with X-linked heredofamilial bilateral microphthalmia (HBM). Three crossovers and 3 non-crossovers were detected in 3 informative matings of 4 generations yielding a recombination value of 0.5. These findings do not provide evidence for linkage between the G6PD and HBM loci, suggesting either that the G6PD and HBM loci are far apart on the X chromosome or that HBM in this family is inherited as an autosomal dominant male sex-limited trait.This publication has 6 references indexed in Scilit:
- X-Linked cataractAnnals of Human Genetics, 1967
- ASSAY OF GLUCOSE-6-PHOSPHATE DEHYDROGENASE (EC1.1.1.49) AND 6-PHOGLUCONAATE DEHYDROGENASE (EC 1.1.1.43) IN RED CELLS1966
- Heredofamilial Bilateral AnophthalmiaArchives of Ophthalmology (1950), 1963
- ELECTROPHORETIC HETEROGENEITY OF GLUCOSE-6-PHOSPHATE DEHYDROGEN ASE AND ITS RELATIONSHIP TO ENZYME DEFICIENCY IN MANProceedings of the National Academy of Sciences, 1962
- SEQUENTIAL TESTS FOR THE DETECTION OF LINKAGE1955
- A CASE OF SEX-LINKED MICROPHTHALMIAJournal of Heredity, 1947