Detection of heterozygous carriers of the Lesch-Nyhan syndrome by electrophoresis of hair root lysates
- 31 March 1973
- journal article
- Published by Elsevier in The Journal of Pediatrics
- Vol. 82 (3), 472-478
- https://doi.org/10.1016/s0022-3476(73)80123-4
Abstract
No abstract availableKeywords
This publication has 13 references indexed in Scilit:
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- Lesch-Nyhan Mutation: Prenatal Detection with Amniotic Fluid CellsScience, 1969
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- Enzyme Defect Associated with a Sex-Linked Human Neurological Disorder and Excessive Purine SynthesisScience, 1967
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