Synpolydactyly: clinical and molecular advances
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.2007.00935.x/fullpdf
Reference34 articles.
1. A large Turkish kindred with syndactyly type II (synpolydactyly). 1. Field investigation, clinical and pedigree data;Sayli;J Med Genet,1995
2. Synpolydactyly phenotypes correlate with size of expansions in HOXD13 polyalanine tract;Goodman;Proc Natl Acad Sci U S A,1997
3. A 72-year-old Danish puzzle resolved-comparative analysis of phenotypes in families with different-sized HOXD13 polyalanine expansions;Kjaer;Am J Med Genet A,2005
4. Synpolydactyly and HOXD13 polyalanine repeat: addition of 2-alanine residues is without clinical consequences;Malik;BMC Med Genet,2007
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