Author:
Jenkinson Emma M.,Rehman Atteeq U.,Walsh Tom,Clayton-Smith Jill,Lee Kwanghyuk,Morell Robert J.,Drummond Meghan C.,Khan Shaheen N.,Naeem Muhammad Asif,Rauf Bushra,Billington Neil,Schultz Julie M.,Urquhart Jill E.,Lee Ming K.,Berry Andrew,Hanley Neil A.,Mehta Sarju,Cilliers Deirdre,Clayton Peter E.,Kingston Helen,Smith Miriam J.,Warner Thomas T.,Black Graeme C.,Trump Dorothy,Davis Julian R.E.,Ahmad Wasim,Leal Suzanne M.,Riazuddin Sheikh,King Mary-Claire,Friedman Thomas B.,Newman William G.
Subject
Genetics (clinical),Genetics
Reference44 articles.
1. The Online London Dysmorphology Database;Guest;Genet. Med.,1999
2. Hereditary hearing loss: from human mutation to mechanism;Lenz;Hear. Res.,2011
3. Deux cas de syndrome de Turner avec surdi-mutite dans une meme fratrie;Perrault;Bull. Mem. Soc. Med. Hop. Paris,1951
4. Perrault syndrome: evidence for progressive nervous system involvement;Fiumara;Am. J. Med. Genet. A.,2004
5. Perrault syndrome: further evidence for genetic heterogeneity;Jenkinson;J. Neurol.,2012
Cited by
196 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