Your browser doesn't support javascript.
loading
A case report of T-box 1 mutation causing phenotypic features of chromosome 22q11.2 deletion syndrome.
Haddad, Raad A; Clines, Gregory A; Wyckoff, Jennifer A.
Afiliación
  • Haddad RA; Division of Metabolism, Endocrinology, and Diabetes (MEND), Department of Internal Medicine, University of Michigan, 24 Frank Lloyd Wright, G-1500, Ann Arbor, MI 48106 USA.
  • Clines GA; Division of Metabolism, Endocrinology, and Diabetes (MEND), Department of Internal Medicine, University of Michigan, 24 Frank Lloyd Wright, G-1500, Ann Arbor, MI 48106 USA.
  • Wyckoff JA; Division of Metabolism, Endocrinology, and Diabetes (MEND), Department of Internal Medicine, University of Michigan, 24 Frank Lloyd Wright, G-1500, Ann Arbor, MI 48106 USA.
Clin Diabetes Endocrinol ; 5: 13, 2019.
Article en En | MEDLINE | ID: mdl-31428446
Palabras clave
Texto completo
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: Clin Diabetes Endocrinol Año: 2019 Tipo del documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: Clin Diabetes Endocrinol Año: 2019 Tipo del documento: Article