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Loss of Tbx1 induces bone phenotypes similar to cleidocranial dysplasia.
Funato, Noriko; Nakamura, Masataka; Richardson, James A; Srivastava, Deepak; Yanagisawa, Hiromi.
Afiliação
  • Funato N; Research Center for Medical and Dental Sciences, Human Gene Sciences Research Division, Tokyo Medical and Dental University, 1-5-45 Yushima, Bunkyo-ku, Tokyo 113-8510, Japan Department of Molecular Biology and.
  • Nakamura M; Research Center for Medical and Dental Sciences, Human Gene Sciences Research Division, Tokyo Medical and Dental University, 1-5-45 Yushima, Bunkyo-ku, Tokyo 113-8510, Japan.
  • Richardson JA; Department of Pathology, University of Texas Southwestern Medical Center, 5323 Harry Hines Blvd., Dallas, TX 75390-9148, USA and.
  • Srivastava D; Gladstone Institute of Cardiovascular Disease and Department of Pediatrics, University of California, San Francisco, 1650 Owens Street, San Francisco, CA 94158, USA.
  • Yanagisawa H; Department of Molecular Biology and hiromi.yanagisawa@utsouthwestern.edu.
Hum Mol Genet ; 24(2): 424-35, 2015 Jan 15.
Article em En | MEDLINE | ID: mdl-25209980
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Osso e Ossos / Displasia Cleidocraniana / Proteínas com Domínio T Limite: Animals / Humans Idioma: En Revista: Hum Mol Genet Ano de publicação: 2015 Tipo de documento: Article
Texto completo
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XML
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Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Osso e Ossos / Displasia Cleidocraniana / Proteínas com Domínio T Limite: Animals / Humans Idioma: En Revista: Hum Mol Genet Ano de publicação: 2015 Tipo de documento: Article