Linkage relationships of X-linked enzymes glucose-6-phosphate dehydrogenase and hypoxanthine guanine phosphoribosyltransferase: recombination in female offspring of compound heterozygotes.

This publication has 29 references indexed in Scilit:

• Detection of heterozygous carriers of the Lesch-Nyhan syndrome by electrophoresis of hair root lysates
  The Journal of Pediatrics, 1973
• Stability of X Chromosomal Inactivation in Human Somatic Cells
  Nature, 1972
• X‐CHROMOSOME INACTIVATION AND DEVELOPMENTAL PATTERNS IN MAMMALS
  Biological Reviews, 1972
• Lesch-Nyhan Syndrome: Rapid Detection of Heterozygotes by Use of Hair Follicles
  Science, 1971
• Genetic Inactivation of the α-Galactosidase Locus in Carriers of Fabry's Disease
  Science, 1970
• Absence of mosaicism in the lymphocyte in X-linked congenital hyperuricosuria
  Life Sciences, 1968
• X-Linked Hypoxanthine-Guanine Phosphoribosyl Transferase Deficiency: Heterozygote Has Two Clonal Populations
  Science, 1968
• HURLER'S SYNDROME: A GENETIC STUDY OF CLONES IN CELL CULTURE WITH PARTICULAR REFERENCE TO THE LYON HYPOTHESIS
  The Journal of Experimental Medicine, 1967
• Enzyme Defect Associated with a Sex-Linked Human Neurological Disorder and Excessive Purine Synthesis
  Science, 1967
• Selection of Hybrids from Matings of Fibroblasts in vitro and Their Presumed Recombinants
  Science, 1964