Split hand foot malformation with whorl-like pigmentary pattern: Phenotypic expression of somatic mosaicism for thep63mutation
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajmg.a.32415/fullpdf
Reference16 articles.
1. EEC syndrome type 3 with a heterozygous germline mutation in the P63 gene and B cell lymphoma;Akahoshi;Am J Med Genet Part A,2003
2. The expanding panorama of split hand foot malformation;Basel;Am J Med Genet Part A,2006
3. Heterozygous germline mutations in the p53 homolog p63 are the cause of EEC syndrome;Celli;Cell,1999
4. P63 mutations are not a major cause of non-syndromic split hand/foot malformation;de Mollerat;J Med Genet,2003
5. An early drawing of Blaschko's lines;Happle;Br J Dermatol,1993
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