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MYRF haploinsufficiency causes 46,XY and 46,XX disorders of sex development: bioinformatics consideration.
Hamanaka, Kohei; Takata, Atsushi; Uchiyama, Yuri; Miyatake, Satoko; Miyake, Noriko; Mitsuhashi, Satomi; Iwama, Kazuhiro; Fujita, Atsushi; Imagawa, Eri; Alkanaq, Ahmed N; Koshimizu, Eriko; Azuma, Yoshiki; Nakashima, Mitsuko; Mizuguchi, Takeshi; Saitsu, Hirotomo; Wada, Yuka; Minami, Sawako; Katoh-Fukui, Yuko; Masunaga, Yohei; Fukami, Maki; Hasegawa, Tomonobu; Ogata, Tsutomu; Matsumoto, Naomichi.
Afiliación
  • Hamanaka K; Department of Human Genetics.
  • Takata A; Department of Human Genetics.
  • Uchiyama Y; Department of Human Genetics.
  • Miyatake S; Department of Oncology.
  • Miyake N; Department of Human Genetics.
  • Mitsuhashi S; Clinical Genetics Department, Yokohama City University Hospital, Yokohama, Kanagawa, Japan.
  • Iwama K; Department of Human Genetics.
  • Fujita A; Department of Human Genetics.
  • Imagawa E; Department of Human Genetics.
  • Alkanaq AN; Department of Human Genetics.
  • Koshimizu E; Department of Human Genetics.
  • Azuma Y; Department of Human Genetics.
  • Nakashima M; Department of Human Genetics.
  • Mizuguchi T; Department of Human Genetics.
  • Saitsu H; Department of Pediatrics, Nagoya University Graduate School of Medicine, Nagoya, Aichi, Japan.
  • Wada Y; Department of Biochemistry, Hamamatsu University School of Medicine, Hamamatsu, Shizuoka, Japan.
  • Minami S; Department of Human Genetics.
  • Katoh-Fukui Y; Department of Biochemistry, Hamamatsu University School of Medicine, Hamamatsu, Shizuoka, Japan.
  • Masunaga Y; Department of Neonatology, National Center for Child Health and Development, Setagaya, Tokyo, Japan.
  • Fukami M; Deparment of Obstetrics and Gynecology, Wakayama Medical University, Wakayama, Wakayama, Japan.
  • Hasegawa T; Department of Molecular Endocrinology, National Center for Child Health and Development, Setagaya, Tokyo, Japan.
  • Ogata T; Department of Pediatrics, Hamamatsu University School of Medicine, Hamamatsu, Shizuoka, Japan.
  • Matsumoto N; Department of Molecular Endocrinology, National Center for Child Health and Development, Setagaya, Tokyo, Japan.
Hum Mol Genet ; 28(14): 2319-2329, 2019 07 15.
Article en En | MEDLINE | ID: mdl-30985895
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Factores de Transcripción / Trastornos del Desarrollo Sexual 46, XX / Trastorno del Desarrollo Sexual 46,XY / Proteínas de la Membrana Tipo de estudio: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adolescent / Adult / Child, preschool / Female / Humans / Male Idioma: En Revista: Hum Mol Genet Asunto de la revista: BIOLOGIA MOLECULAR / GENETICA MEDICA Año: 2019 Tipo del documento: Article
Texto completo
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Factores de Transcripción / Trastornos del Desarrollo Sexual 46, XX / Trastorno del Desarrollo Sexual 46,XY / Proteínas de la Membrana Tipo de estudio: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adolescent / Adult / Child, preschool / Female / Humans / Male Idioma: En Revista: Hum Mol Genet Asunto de la revista: BIOLOGIA MOLECULAR / GENETICA MEDICA Año: 2019 Tipo del documento: Article