Genetic heterogeneity in type III familial cutaneous syndactyly and linkage to chromosome 7q36
Author:
Affiliation:
1. Department of Surgery; College of Medicine, King Saud University; Riyadh; Saudi Arabia
2. Department of Genetics; King Faisal Specialist Hospital and Research Center; Riyadh; Saudi Arabia
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajmg.a.35956/fullpdf
Reference21 articles.
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3. Type II familial synpolydactyly: Report on two families with an emphasis on variations of expression;Al-Qattan;Eur J Human Genet,2011
4. A novel mutation in the SHH long-range regulator (ZRS) is associated with preaxial polydactyly, triphalangeal thumb, and severe radial ray deficiency;Al-Qattan;Am J Med Genet Part A,2012
5. Syndactyly: Frequency of specific types;Castilla;Am J Med Genet,1980
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