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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...

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Detalhes bibliográficos
Publicado no:Eur J Hum Genet
Main Authors: Rafique, Muhammad Arshad, Ansar, Muhammad, Jamal, Syed Muhammad, Malik, Sajid, Sohail, Muhammad, Faiyaz-Ul-Haque, Mohammad, Haque, Sayedul, Leal, Suzanne M, Ahmad, Wasim
Formato: Artigo
Idioma:Inglês
Publicado em: 2003
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Acesso em linha: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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