Identification of the gene for Nance-Horan syndrome (NHS)

Background: The disease intervals for Nance-Horan syndrome (NHS [MIM 302350]) and X linked congenital cataract (CXN) overlap on Xp22. Objective: To identify the gene or genes responsible for these diseases. Methods: Families with NHS were ascertained. The refined locus for CXN was used to focus the...

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Detaylı Bibliyografya
Asıl Yazarlar: Brooks, S, Ebenezer, N, Poopalasundaram, S, Lehmann, O, Moore, A, Hardcastle, A
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: BMJ Group 2004
Konular:
Short Report
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC1735593/
https://ncbi.nlm.nih.gov/pubmed/15466011
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/jmg.2004.022517
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