WNT10A mutations are a frequent cause of a broad spectrum of ectodermal dysplasias with sex-biased manifestation pattern in heterozygotes. | Am J Hum Genet;85(1): 97-105, 2009 Jul. | MEDLINE

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WNT10A mutations are a frequent cause of a broad spectrum of ectodermal dysplasias with sex-biased manifestation pattern in heterozygotes.

Bohring, Axel; Stamm, Thomas; Spaich, Christiane; Haase, Claudia; Spree, Kerstin; Hehr, Ute; Hoffmann, Mandy; Ledig, Susanne; Sel, Saadettin; Wieacker, Peter; Röpke, Albrecht.

Affiliation

Bohring A; Institut für Humangenetik, Westfälische Wilhelms-Universität, 48149 Münster, Germany. abohring@aol.com

Am J Hum Genet ; 85(1): 97-105, 2009 Jul.

Article in En | MEDLINE | ID: mdl-19559398

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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Ectodermal Dysplasia / Wnt Proteins / Mutation Limits: Female / Humans / Male Language: En Journal: Am J Hum Genet Year: 2009 Document type: Article Affiliation country: Alemania Country of publication: Estados Unidos

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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Ectodermal Dysplasia / Wnt Proteins / Mutation Limits: Female / Humans / Male Language: En Journal: Am J Hum Genet Year: 2009 Document type: Article Affiliation country: Alemania Country of publication: Estados Unidos