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Fragile x-associated premature ovarian failure in a large Turkish cohort: Findings of Hacettepe Fragile X Registry.
Utine, Gülen Eda; Simsek-Kiper, Pelin Özlem; Akgün-Dogan, Özlem; Ürel-Demir, Gizem; Alanay, Yasemin; Aktas, Dilek; Boduroglu, Koray; Tunçbilek, Ergül; Alikasifoglu, Mehmet.
Afiliación
  • Utine GE; Hacettepe University, Faculty of Medicine, Department of Pediatrics, Department of Pediatric Genetics, Ankara, Turkey. Electronic address: geutine@hacettepe.edu.tr.
  • Simsek-Kiper PÖ; Hacettepe University, Faculty of Medicine, Department of Pediatrics, Department of Pediatric Genetics, Ankara, Turkey.
  • Akgün-Dogan Ö; Hacettepe University, Faculty of Medicine, Department of Pediatrics, Department of Pediatric Genetics, Ankara, Turkey.
  • Ürel-Demir G; Hacettepe University, Faculty of Medicine, Department of Pediatrics, Department of Pediatric Genetics, Ankara, Turkey.
  • Alanay Y; Hacettepe University, Faculty of Medicine, Department of Pediatrics, Department of Pediatric Genetics, Ankara, Turkey; Acibadem University, School of Medicine, Department of Pediatrics, Pediatric Genetics Unit, Istanbul, Turkey.
  • Aktas D; Hacettepe University, Faculty of Medicine, Department of Pediatrics, Department of Pediatric Genetics, Ankara, Turkey.
  • Boduroglu K; Hacettepe University, Faculty of Medicine, Department of Pediatrics, Department of Pediatric Genetics, Ankara, Turkey.
  • Tunçbilek E; Hacettepe University, Faculty of Medicine, Department of Pediatrics, Department of Pediatric Genetics, Ankara, Turkey.
  • Alikasifoglu M; Hacettepe University, Faculty of Medicine, Department of Pediatrics, Department of Pediatric Genetics, Ankara, Turkey.
Eur J Obstet Gynecol Reprod Biol ; 221: 76-80, 2018 Feb.
Article en En | MEDLINE | ID: mdl-29275276
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Insuficiencia Ovárica Primaria / Proteína de la Discapacidad Intelectual del Síndrome del Cromosoma X Frágil / Síndrome del Cromosoma X Frágil / Mutación Tipo de estudio: Diagnostic_studies / Etiology_studies / Incidence_studies / Observational_studies / Risk_factors_studies País/Región como asunto: Asia Idioma: En Revista: Eur J Obstet Gynecol Reprod Biol Año: 2018 Tipo del documento: Article
Texto completo
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Insuficiencia Ovárica Primaria / Proteína de la Discapacidad Intelectual del Síndrome del Cromosoma X Frágil / Síndrome del Cromosoma X Frágil / Mutación Tipo de estudio: Diagnostic_studies / Etiology_studies / Incidence_studies / Observational_studies / Risk_factors_studies País/Región como asunto: Asia Idioma: En Revista: Eur J Obstet Gynecol Reprod Biol Año: 2018 Tipo del documento: Article