Author:
Rupp Verena,Rauf Sobiah,Naveed Ishrat,Windpassinger Christian,Mir Asif
Publisher
Springer Science and Business Media LLC
Subject
Genetics (clinical),Genetics
Reference39 articles.
1. Passemard S, Kaindl AM, Titomanlio L, Gerard B, Gressens P: Primary autosomal recessive microcephaly. GeneReviews. Edited by: Pagon RA, Bird TD, Dolan CR, Stephens K. 1993, University of Washington, Seattle, Seattle (WA)
2. Roberts E, Hampshire DJ, Pattison L, Springell K, Jafri H: Autosomal recessive primary microcephaly: an analysis of locus heterogeneity and phenotypic variation. J Med Genet. 2002, 39: 718-721. 10.1136/jmg.39.10.718.
3. Thornton GK, Woods CG: Primary microcephaly: do all roads lead to rome?. Trends Genet. 2009, 25: 501-510. 10.1016/j.tig.2009.09.011.
4. Awad S, Al-Dosari MS, Al-Yacoub N, Colak D, Salih MA: Mutation in PHC1 implicates chromatin remodeling in primary microcephaly pathogenesis. Hum Mol Genet. 2013, 22: 22002213-10.1093/hmg/ddt072.
5. Bilguvar K, Ozturk AK, Louvi A, Kwan KY, Choi M, Tatli B, Yalnızoğlu D, Tüysüz B, Çağlayan AO, Gökben S, Kaymakçalan H, Barak T, Bakırcıoğlu M, Yasuno K, Ho W, Sanders S, Zhu Y, Yılmaz S, Dinçer A, Johnson MH, Bronen RA, Koçer N, Per H, Mane S, Pamir MN, Yalçınkaya C, Kumandaş S, Topçu M, Özmen M, Sestan N, et al: Whole-exome sequencing identifies recessive WDR62 mutations in severe brain malformations. Nature. 2010, 467: 207-210. 10.1038/nature09327.
Cited by
11 articles.
订阅此论文施引文献
订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献