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A rare cause of primary amenorrhea: LHCGR gene mutations.
Aktar Karakaya, Amine; Çayir, Atilla; Unal, Edip; Bestas, Asli; Ece Solmaz, Asli; Kenan Haspolat, Yusuf.
Afiliação
  • Aktar Karakaya A; Department of Pediatric Endocrinology, Faculty of Medicine, Dicle University, Diyarbakir, Turkey. Electronic address: aktarkarakaya@gmail.com.
  • Çayir A; Department of Pediatric Endocrinology, Erzurum Regional Training and Research Hospital Erzurum, Turkey.
  • Unal E; Department of Pediatric Endocrinology, Faculty of Medicine, Dicle University, Diyarbakir, Turkey.
  • Bestas A; Department of Pediatric Endocrinology, Faculty of Medicine, Dicle University, Diyarbakir, Turkey.
  • Ece Solmaz A; Department of Medical Genetics, Faculty of Medicine, Ege University, Izmir, Turkey.
  • Kenan Haspolat Y; Department of Pediatric Endocrinology, Faculty of Medicine, Dicle University, Diyarbakir, Turkey.
Eur J Obstet Gynecol Reprod Biol ; 272: 193-197, 2022 May.
Article em En | MEDLINE | ID: mdl-35366614
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Receptores do LH / Amenorreia Tipo de estudo: Observational_studies Limite: Female / Humans / Male Idioma: En Revista: Eur J Obstet Gynecol Reprod Biol Ano de publicação: 2022 Tipo de documento: Article
Texto completo
Adicionar na Minha BVS
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Receptores do LH / Amenorreia Tipo de estudo: Observational_studies Limite: Female / Humans / Male Idioma: En Revista: Eur J Obstet Gynecol Reprod Biol Ano de publicação: 2022 Tipo de documento: Article