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Early decline in functional ovarian reserve in young women with low (CGGn < 26) FMR1 gene alleles.
Gleicher, Norbert; Yu, Yao; Himaya, Erik; Barad, David H; Weghofer, Andrea; Wu, Yan-Guang; Albertini, David F; Wang, Vicki Qi; Kushnir, Vitaly A.
Afiliación
  • Gleicher N; Center for Human Reproduction, New York, NY; Foundation for Reproductive Medicine, New York, NY; Stem Cell Biology and Molecular Embryology Laboratory, The Rockefeller University, New York, NY. Electronic address: ykizawa@thechr.com.
  • Yu Y; Center for Human Reproduction, New York, NY.
  • Himaya E; Gatineau Hospital, McGill University, Montréal, Quebec, Canada.
  • Barad DH; Center for Human Reproduction, New York, NY; Foundation for Reproductive Medicine, New York, NY; Department of Obstetrics and Gynecology, Albert Einstein College of Medicine, Bronx, NY.
  • Weghofer A; Center for Human Reproduction, New York, NY; Department of Obstetrics and Gynecology, University of Vienna School of Medicine, Vienna, Austria.
  • Wu YG; Center for Human Reproduction, New York, NY.
  • Albertini DF; Center for Human Reproduction, New York, NY; Department of Molecular and Integrative Physiology, University of Kansas School of Medicine, Wichita, KS.
  • Wang VQ; Center for Human Reproduction, New York, NY.
  • Kushnir VA; Center for Human Reproduction, New York, NY; Department of Obstetrics and Gynecology, Wake Forest School of Medicine, Winston-Salem, NC.
Transl Res ; 166(5): 502-7.e1-2, 2015 Nov.
Article en En | MEDLINE | ID: mdl-26209748

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Alelos / Proteína de la Discapacidad Intelectual del Síndrome del Cromosoma X Frágil / Reserva Ovárica Tipo de estudio: Observational_studies / Risk_factors_studies Límite: Adult / Female / Humans Idioma: En Revista: Transl Res Asunto de la revista: MEDICINA / TECNICAS E PROCEDIMENTOS DE LABORATORIO Año: 2015 Tipo del documento: Article Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Alelos / Proteína de la Discapacidad Intelectual del Síndrome del Cromosoma X Frágil / Reserva Ovárica Tipo de estudio: Observational_studies / Risk_factors_studies Límite: Adult / Female / Humans Idioma: En Revista: Transl Res Asunto de la revista: MEDICINA / TECNICAS E PROCEDIMENTOS DE LABORATORIO Año: 2015 Tipo del documento: Article Pais de publicación: Estados Unidos