Mapping of monilethrix to the type II keratin gene cluster at chromosome 12q13 in three new families, including one with variable expressivity
Author:
Publisher
Wiley
Subject
Dermatology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1046/j.1365-2133.1997.18461954.x/fullpdf
Reference25 articles.
1. A rare nodose condition of the hair;Smith;Br Med J,1879
2. Monilethrix and Pseudo-Monilethrix
3. Monilethrix: an electron microscopic and electron histochemical study;Gummer;Br J Dermatol,1981
4. Pathogenesis of monilethrix: computer stereography and electron microscopy;Ito;J Invest Dermatol,1990
5. Monilethrix: a clinicopathological illustration of a cortical defect;Berker;Br J Dermatol,1993
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1. Severe Monilethrix Associated with Intractable Scalp Pruritus, Posterior Subcapsular Cataract, Brachiocephaly, and Distinct Facial Features: A New Variant of Monilethrix Syndrome?;Pediatric Dermatology;2004-07
2. De novo mutations in monilethrix;Experimental Dermatology;2003-12
3. Recurrent missense mutations in the hair keratin gene hHb6 in monilethrix;Clinical and Experimental Dermatology;2003-03
4. Brief communication. The hypotrichosis-generating shorn (shn) mutation maps to distal chromosome 7 in the Norway rat;Journal of Heredity;2000-07
5. Monilethrix?Improvement by Hormonal�Influences?;Pediatric Dermatology;1999-07
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