Author:
Agha Zehra,Iqbal Zafar,Azam Maleeha,Hoefsloot Lies H.,van Bokhoven Hans,Qamar Raheel
Funder
HEC NRPU
COMSATS Institute of Information Technology
European Union's Seventh Framework Program
Higher Education Commission
Subject
Genetics,General Medicine
Reference31 articles.
1. Basal body dysfunction is a likely cause of pleiotropic Bardet–Biedl syndrome;Ansley;Nature,2003
2. Identification of a novel Bardet–Biedl syndrome protein, BBS7, that shares structural features with BBS1 and BBS2;Badano;Am. J. Hum. Genet.,2003
3. Dissection of epistasis in oligogenic Bardet–Biedl syndrome;Badano;Nature,2006
4. New criteria for improved diagnosis of Bardet–Biedl syndrome: results of a population survey;Beales;J. Med. Genet.,1999
5. Molecular analysis of Bardet–Biedl syndrome families: report of 21 novel mutations in 10 genes;Chen;IOVS,2011
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