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A locus for hereditary hypotrichosis localized to human chromosome 18q21.1

Hereditary hypotrichosis is a rare autosomal recessive condition characterized clinically by alopecia. Three consanguineous kindreds with multiple affected individuals were ascertained from different regions of Pakistan. A novel hypotrichosis locus was mapped to a 5.5 cM region on chromosome 18q21.1...

詳細記述

保存先:
書誌詳細
出版年:Eur J Hum Genet
主要な著者: Rafique, Muhammad Arshad, Ansar, Muhammad, Jamal, Syed Muhammad, Malik, Sajid, Sohail, Muhammad, Faiyaz-Ul-Haque, Mohammad, Haque, Sayedul, Leal, Suzanne M, Ahmad, Wasim
フォーマット: Artigo
言語:Inglês
出版事項: 2003
主題:
オンライン・アクセス:https://ncbi.nlm.nih.gov/pmc/articles/PMC6157268/
https://ncbi.nlm.nih.gov/pubmed/12891384
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/sj.ejhg.5201005
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