» Articles » PMID: 2516183

Hair Root Diagnosis of Fabry's Disease

Overview
Publisher Wiley
Date 1989 Jan 1
PMID 2516183
Authors
Affiliations
Soon will be listed here.
References
1.
Ejiofor A, Robinson D, Wise D, Hamers M, Tager J . Anderson-Fabry disease: rapid detection of carriers by hair bulb analysis. J Inherit Metab Dis. 1978; 1(2):71-4. DOI: 10.1007/BF01801848. View

2.
Grimm T, Wienker T, Ropers H . Fabry's disease: heterozygote detection by hair root analysis. Hum Genet. 1976; 32(3):329-34. DOI: 10.1007/BF00295824. View

3.
Spence M, Goldbloom A, Burgess J, DEntremont D, Ripley B, Weldon K . Heterozygote detection in angiokeratoma corporis diffusum (Anderson-Fabry disease). Studies on plasma, leucocytes, and hair follicles. J Med Genet. 1977; 14(2):91-9. PMC: 1013521. DOI: 10.1136/jmg.14.2.91. View

4.
de Bruyn C, Vermorken A, Oei T, GEERTS S . Inborn errors of metabolism: screening for heterozygotes using hair roots. Br J Dermatol. 1979; 101(1):111-4. DOI: 10.1111/j.1365-2133.1979.tb15302.x. View

5.
Hatton C, Cooper A, Sardharwalla I . Detection of Fabry's disease carriers by enzyme assay of hair roots. J Inherit Metab Dis. 1989; 12 Suppl 2:369-71. DOI: 10.1007/BF03335425. View