Studies of skin fibroblasts from 10 families with HGPRT deficiency, with reference in X-chromosomal inactivation.
- 1 March 1971
- journal article
- Vol. 23 (2), 199-210
Abstract
No abstract availableThis publication has 18 references indexed in Scilit:
- Diploid Azaguanine-Resistant Mutants of Cultured Human FibroblastsScience, 1970
- Purine Metabolism in Heterozygous Carriers of Hypoxanthine-Guanine Phosphoribosyltransferase DeficiencyScience, 1969
- Absence of mosaicism in the lymphocyte in X-linked congenital hyperuricosuriaLife Sciences, 1968
- X-Linked Hypoxanthine-Guanine Phosphoribosyl Transferase Deficiency: Heterozygote Has Two Clonal PopulationsScience, 1968
- HURLER'S SYNDROME: A GENETIC STUDY OF CLONES IN CELL CULTURE WITH PARTICULAR REFERENCE TO THE LYON HYPOTHESISThe Journal of Experimental Medicine, 1967
- A familial disorder of uric acid metabolism and central nervous system functionAmerican Journal Of Medicine, 1964
- Genetic Tests with a Sex-Linked Marker: Glucose-6-Phosphate DehydrogenaseCold Spring Harbor Symposia on Quantitative Biology, 1964
- Selection in Mammalian Mosaic Cell PopulationsCold Spring Harbor Symposia on Quantitative Biology, 1964
- Mammalian X-Chromosome Action: Inactivation Limited in Spread and in Region of OriginScience, 1963
- Gene Action in the X-chromosome of the Mouse (Mus musculus L.)Nature, 1961