Localization of loci for hypoxanthine phosphoribosyltransferase and glucose-6-phosphate dehydrogenase and biochemical evidence of nonrandom X chromosome expression from studies of a human X-autosome translocation.

समान संसाधन

• Fragile X syndrome: search for phenotypic manifestations at loci for hypoxanthine phosphoribosyltransferase and glucose-6-phosphate dehydrogenase.
  द्वारा: Mareni, C, और अन्य
  प्रकाशित: (1981)
• Methylation of the hypoxanthine phosphoribosyltransferase locus on the human X chromosome: implications for X-chromosome inactivation.
  द्वारा: Wolf, S F, और अन्य
  प्रकाशित: (1984)
• Linkage relationships of X-linked enzymes glucose-6-phosphate dehydrogenase and hypoxanthine guanine phosphoribosyltransferase: recombination in female offspring of compound heterozygotes.
  द्वारा: Francke, U, और अन्य
  प्रकाशित: (1974)
• Clinical and biochemical observations on three cases of hypoxanthine-guanine phosphoribosyltransferase deficiency.
  द्वारा: Bunn, D N, और अन्य
  प्रकाशित: (1975)
• Comparative Studies on X-Autosome Translocations in the Mouse. II. Inactivation of Autosomal Loci, Segregation, and Mapping of Autosomal Breakpoints in Five T(x;1)'s
  द्वारा: Russell, Liane Brauch, और अन्य
  प्रकाशित: (1970)