Your browser doesn't support javascript.
loading
Refining the risk for fragile X-associated primary ovarian insufficiency (FXPOI) by FMR1 CGG repeat size.
Allen, Emily Graves; Charen, Krista; Hipp, Heather S; Shubeck, Lisa; Amin, Ashima; He, Weiya; Nolin, Sarah L; Glicksman, Anne; Tortora, Nicole; McKinnon, Bonnie; Shelly, Katharine E; Sherman, Stephanie L.
Afiliación
  • Allen EG; Department of Human Genetics, Emory University School of Medicine, Atlanta, GA, USA. emgrave@emory.edu.
  • Charen K; Department of Human Genetics, Emory University School of Medicine, Atlanta, GA, USA.
  • Hipp HS; Department of Gynecology and Obstetrics, Emory University School of Medicine, Atlanta, GA, USA.
  • Shubeck L; Department of Human Genetics, Emory University School of Medicine, Atlanta, GA, USA.
  • Amin A; Department of Human Genetics, Emory University School of Medicine, Atlanta, GA, USA.
  • He W; Department of Human Genetics, Emory University School of Medicine, Atlanta, GA, USA.
  • Nolin SL; Department of Human Genetics, New York State Institute for Basic Research in Developmental Disabilities, Staten Island, NY, USA.
  • Glicksman A; Department of Human Genetics, New York State Institute for Basic Research in Developmental Disabilities, Staten Island, NY, USA.
  • Tortora N; Department of Human Genetics, New York State Institute for Basic Research in Developmental Disabilities, Staten Island, NY, USA.
  • McKinnon B; Department of Human Genetics, Emory University School of Medicine, Atlanta, GA, USA.
  • Shelly KE; Department of Human Genetics, Emory University School of Medicine, Atlanta, GA, USA.
  • Sherman SL; Department of Human Genetics, Emory University School of Medicine, Atlanta, GA, USA.
Genet Med ; 23(9): 1648-1655, 2021 09.
Article en En | MEDLINE | ID: mdl-33927378
Asunto(s)
Texto completo
Añadir a Mi BVS
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Menopausia Prematura / Insuficiencia Ovárica Primaria / Síndrome del Cromosoma X Frágil Tipo de estudio: Etiology_studies / Prognostic_studies / Risk_factors_studies Límite: Female / Humans Idioma: En Revista: Genet Med Asunto de la revista: GENETICA MEDICA Año: 2021 Tipo del documento: Article País de afiliación: Estados Unidos
Texto completo
Añadir a Mi BVS
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Menopausia Prematura / Insuficiencia Ovárica Primaria / Síndrome del Cromosoma X Frágil Tipo de estudio: Etiology_studies / Prognostic_studies / Risk_factors_studies Límite: Female / Humans Idioma: En Revista: Genet Med Asunto de la revista: GENETICA MEDICA Año: 2021 Tipo del documento: Article País de afiliación: Estados Unidos