Author:
Hayat Amir,Khan Atif Ahmad,Rauf Abdur,Khan Saad Ullah,Hussain Shabir,Ullah Asmat,Ahmad Wasim,Shams Sulaiman,Khan Bushra
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
Genetics (clinical),General Medicine,Pathology and Forensic Medicine,Anatomy,Pediatrics, Perinatology and Child Health
Reference39 articles.
1. IFT27, encoding a small gtpase component of IFT particles, is mutated in a consanguineous family with Bardet-Biedl syndrome.;Aldahmesh;Hum Mol Genet,2014
2. Basal body dysfunction is a likely cause of pleiotropic Bardet-Biedl syndrome.;Ansley;Nature,2003
3. Identification of a novel Bardet-Biedl syndrome protein, BBS7, that shares structural features with BBS1 and BBS2.;Badano;Am J Hum Genet,2003
4. New criteria for improved diagnosis of Bardet-Biedl syndrome: results of a population survey.;Beales;J Med Genet,1999
5. Homozygosity mapping with SNP arrays identifies TRIM32, an E3 ubiquitin ligase, as a Bardet-Biedl syndrome gene (BBS11).;Chiang;Proc Natl Acad Sci U S A,2006
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