Heterozygote detection in Fabry's disease using mailed hair roots
- 1 July 1980
- journal article
- Published by Oxford University Press (OUP) in British Journal of Dermatology
- Vol. 103 (1) , 101-103
- https://doi.org/10.1111/j.1365-2133.1980.tb15845.x
Abstract
No abstract availableThis publication has 7 references indexed in Scilit:
- Anderson‐fabry disease: Rapid detection of carriers by hair bulb analysisJournal of Inherited Metabolic Disease, 1978
- Detection of Fabry's disease heterozygotes by hair root analysisClinical Genetics, 1978
- Fabry's disease: biochemical and histochemical studies on hair roots for carrier detectionBritish Journal of Dermatology, 1978
- HAIR-ROOTS IN SCREENING AND DIAGNOSIS OF TAY-SACHS DISEASEThe Lancet, 1977
- Fabry's disease: Heterozygote detection by hair root analysisHuman Genetics, 1976
- Studies on hair roots for carrier detection in hypoxanthine‐guanine phosphoribosyl transferase deficiencyClinical Genetics, 1974
- Lesch-Nyhan Syndrome: Rapid Detection of Heterozygotes by Use of Hair FolliclesScience, 1971