Chargement en cours...

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...

Description complète

Enregistré dans:
Détails bibliographiques
Publié dans:Eur J Hum Genet
Auteurs principaux: Rafique, Muhammad Arshad, Ansar, Muhammad, Jamal, Syed Muhammad, Malik, Sajid, Sohail, Muhammad, Faiyaz-Ul-Haque, Mohammad, Haque, Sayedul, Leal, Suzanne M, Ahmad, Wasim
Format: Artigo
Langue:Inglês
Publié: 2003
Sujets:
Accès en ligne: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
Tags: Ajouter un tag
Pas de tags, Soyez le premier à ajouter un tag!