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MAP3K1-related gonadal dysgenesis: Six new cases and review of the literature.
Granados, Andrea; Alaniz, Veronica I; Mohnach, Lauren; Barseghyan, Hayk; Vilain, Eric; Ostrer, Harry; Quint, Elisabeth H; Chen, Ming; Keegan, Catherine E.
Afiliação
  • Granados A; Department of Pediatrics, Division of Endocrinology, University of Michigan, Ann Arbor, Michigan.
  • Alaniz VI; Department of Obstetrics and Gynecology, University of Michigan, Ann Arbor, Michigan.
  • Mohnach L; Disorder of Sex Development Program, University of Michigan, Ann Arbor, Michigan.
  • Barseghyan H; Department of Human Genetics, UCLA, Los Angeles, California.
  • Vilain E; Department of Human Genetics, UCLA, Los Angeles, California.
  • Ostrer H; Departments of Pathology and Pediatrics, Albert Einstein College of Medicine, Bronx, New York.
  • Quint EH; Department of Obstetrics and Gynecology, University of Michigan, Ann Arbor, Michigan.
  • Chen M; Department of Pediatrics, Division of Endocrinology, University of Michigan, Ann Arbor, Michigan.
  • Keegan CE; Department of Pediatrics, Division of Genetics and Department of Human Genetics, University of Michigan, Ann Arbor, Michigan.
Am J Med Genet C Semin Med Genet ; 175(2): 253-259, 2017 06.
Article em En | MEDLINE | ID: mdl-28504475
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Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Diferenciação Sexual / MAP Quinase Quinase Quinase 1 / Transtorno 46,XY do Desenvolvimento Sexual / Disgenesia Gonadal Limite: Adolescent / Child / Child, preschool / Female / Humans / Male Idioma: En Revista: Am J Med Genet C Semin Med Genet Assunto da revista: GENETICA MEDICA Ano de publicação: 2017 Tipo de documento: Article
Texto completo
Adicionar na Minha BVS
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Diferenciação Sexual / MAP Quinase Quinase Quinase 1 / Transtorno 46,XY do Desenvolvimento Sexual / Disgenesia Gonadal Limite: Adolescent / Child / Child, preschool / Female / Humans / Male Idioma: En Revista: Am J Med Genet C Semin Med Genet Assunto da revista: GENETICA MEDICA Ano de publicação: 2017 Tipo de documento: Article