Homozygous WNT10b mutation and complex inheritance in Split-Hand/Foot Malformation
Author:
Publisher
Oxford University Press (OUP)
Subject
Genetics(clinical),Genetics,Molecular Biology,General Medicine
Link
http://academic.oup.com/hmg/article-pdf/17/17/2644/17245104/ddn164.pdf
Reference30 articles.
1. Pathogenesis of split-hand/split-foot malformation;Duijf;Hum. Mol. Genet.,2003
2. Split-Hand-Foot-Malformation (SHFM);Elliott;Clin. Genet.,2005
3. Fine mapping of the autosomal dominant split hand/split foot locus on chromosome 7, band q21.3-q22.1;Scherer;Am. J. Hum. Genet.,1994
4. The 10q24-linked split hand/split foot syndrome (SHFM3): narrowing of the critical region and confirmation of the clinical phenotype;Roscioli;Am. J. Med. Genet.,2004
5. Split-hand/split-foot malformation is caused by mutations in the p63 gene on 3q27;Ianakiev;Am. J. Hum. Genet.,2000
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