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Lesch-Nyhan Syndrome: Rapid Detection of Heterozygotes by Use of Hair Follicles

published in: Science

date of publication: 1971-05-01

language: English

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Cites articles 10

Date

Title

Authors

1958-07-01

Dependence of bone marrow cells on the liver for purine supply
1964-04

A FAMILIAL DISORDER OF URIC ACID METABOLISM AND CENTRAL NERVOUS SYSTEM FUNCTION
1964-10-01

ION-EXCHANGE CHROMATOGRAPHY OF NUCLEOTIDES ON POLY-(ETHYLENEIMINE)-CELLULOSE THIN LAYERS
1967-03-31

Enzyme Defect Associated with a Sex-Linked Human Neurological Disorder and Excessive Purine Synthesis,Enzyme defect associated with a sex-linked human neurological disorder and excessive purine synthesis
1968-04-01

X-linked hypoxanthine-guanine phosphoribosyl transferase deficiency: heterozygote has two clonal populations
1968-06-01

Single-allele expression at an X-linked hyperuricemia locus in heterozygous human cells
1969-10-01

Glucose-6 phosphate dehydrogenase mosaicism: utilization as a tracer in the study of the development of hair root cells
1970-06-01

X-linked hypoxanthine-guanine phosphoribosyl transferase deficiency: detection of heterozygotes by selective medium,X-linked hypoxanthine-guanine phosphoribosyl transferase deficiency: Detection of heterozygotes by selective medium
1970-01-01

Hemizygous expression of glucose-6-phosphate dehydrogenase in erythrocytes of heterozygotes for the Lesch-Nyhan syndrome
Clinical Genetics

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