WNT9B in 542 Chinese women with Müllerian duct abnormalities: mutation analysis.

Tang, Rong; Dang, Yujie; Qin, Yingying; Zou, Shuhua; Li, Guangyu; Wang, Yu; Chen, Zi-Jiang

Tang, Rong; Dang, Yujie; Qin, Yingying; Zou, Shuhua; Li, Guangyu; Wang, Yu; Chen, Zi-Jiang.

Afiliação

Tang R; Center for Reproductive Medicine, Provincial Hospital Affiliated with Shandong University, Jinan 250021, China; National Research Center for Assisted Reproductive Technology and Reproductive Genetics, 250021, China; The Key Laboratory for Reproductive Endocrinology of Ministry of Education, 250021,
Dang Y; Center for Reproductive Medicine, Provincial Hospital Affiliated with Shandong University, Jinan 250021, China; National Research Center for Assisted Reproductive Technology and Reproductive Genetics, 250021, China; The Key Laboratory for Reproductive Endocrinology of Ministry of Education, 250021,
Qin Y; Center for Reproductive Medicine, Provincial Hospital Affiliated with Shandong University, Jinan 250021, China; National Research Center for Assisted Reproductive Technology and Reproductive Genetics, 250021, China; The Key Laboratory for Reproductive Endocrinology of Ministry of Education, 250021,
Zou S; Qingdao Women and Children Medical Healthcare Center, Qingdao 266000, China.
Li G; Center for Reproductive Medicine, Provincial Hospital Affiliated with Shandong University, Jinan 250021, China; National Research Center for Assisted Reproductive Technology and Reproductive Genetics, 250021, China; The Key Laboratory for Reproductive Endocrinology of Ministry of Education, 250021,
Wang Y; Center for Reproductive Medicine, Renji Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
Chen ZJ; Center for Reproductive Medicine, Provincial Hospital Affiliated with Shandong University, Jinan 250021, China; National Research Center for Assisted Reproductive Technology and Reproductive Genetics, 250021, China; The Key Laboratory for Reproductive Endocrinology of Ministry of Education, 250021,

Reprod Biomed Online ; 28(4): 503-7, 2014 Apr.

Article em En | MEDLINE | ID: mdl-24581601

Assuntos

Povo Asiático/genética; Ductos Paramesonéfricos/anormalidades; Proteínas Wnt/genética; China; Feminino; Humanos; Polimorfismo de Nucleotídeo Único

Palavras-chave

MRKH syndrome; Müllerian duct abnormalities; WNT9B; mutation; single-nucleotide polymorphisms; synonymous

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Povo Asiático / Proteínas Wnt / Ductos Paramesonéfricos Tipo de estudo: Prognostic_studies Limite: Female / Humans País/Região como assunto: Asia Idioma: En Revista: Reprod Biomed Online Assunto da revista: MEDICINA REPRODUTIVA Ano de publicação: 2014 Tipo de documento: Article

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