Fabry's disease: biochemical and histochemical studies on hair roots for carrier detection
Author:
Publisher
Wiley
Subject
Dermatology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2133.1978.tb01621.x/fullpdf
Reference8 articles.
1. Studies on hair roots for carrier detection in hypoxanthine-guanine phosphoribosyl transferase deficiency
2. Lesch-Nyhan Syndrome: Rapid Detection of Heterozygotes by Use of Hair Follicles
3. Fabry's disease: Heterozygote detection by hair root analysis
4. HAIR-ROOTS IN SCREENING AND DIAGNOSIS OF TAY-SACHS DISEASE
5. Z. Lojda, R. Gossrau, and T. H. Schiebler(1976 ) Enzym-histochemische Methoden , I. edn. , p. 127 , Springer-Verlag, Berlin.
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1. Immunofluorescence imaging diagnosis of Fabry heterozygotes using confocal laser scanning microscopy;Clinical Genetics;2008-04-23
2. Human hair follicles may be used for population screening of heterozygotes of glucose-6-phosphate dehydrogenase deficiency;Clinical Genetics;2008-04-23
3. Heterozygote detection in glucose-6-phosphate dehydrogenase deficiency: limitation of hair follicle analysis;Clinical Genetics;2008-04-23
4. Differentiation of hair growth cycle from scalp hair roots for the diagnosis of glucose-6-phosphate dehydrogenase deficiency in neonates;Journal of Inherited Metabolic Disease;2000-11
5. Noninvasive Test for Fragile X Syndrome, Using Hair Root Analysis;The American Journal of Human Genetics;1999-07
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