WNT10A and isolated hypodontia
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajmg.a.33840/fullpdf
Reference20 articles.
1. Mutation in WNT10A is associated with an autosomal recessive ectodermal dysplasia: The odonto-onycho-dermal dysplasia;Adaimy;Am J Hum Genet,2007
2. WNT10A mutations are a frequent cause of a broad spectrum of ectodermal dysplasias with sex-biased manifestation pattern in heterozygotes;Bohring;Am J Hum Genet,2009
3. Schöpf-Schulz-Passarge syndrome: Further delineation of the phenotype and genetic considerations;Castori;Acta Derm Venereol,2008
4. Molecular dimensions of gastrointestinal tumors: Some thoughts for digestion;Cohen;Am J Med Genet Part A,2003
5. The new bone biology: Pathologic, molecular, and clinical correlates;Cohen;Am J Med Genet Part A,2006
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