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Evidence for HNRNPH1 being another gene for Bain type syndromic mental retardation.
Pilch, Jacek; Koppolu, Agnieszka A; Walczak, Anna; Murcia Pienkowski, Victor A; Biernacka, Anna; Skiba, Pawel; Machnik-Broncel, Joanna; Gasperowicz, Piotr; Kosinska, Joanna; Rydzanicz, Malgorzata; Emich-Widera, Ewa; Ploski, Rafal.
Afiliación
  • Pilch J; Department of Pediatric Neurology, Medical University of Silesia, Katowice, Poland.
  • Koppolu AA; Department of Medical Genetics, Medical University of Warsaw, Warsaw, Poland.
  • Walczak A; Postgraduate School of Molecular Medicine, Medical University of Warsaw, Warsaw, Poland.
  • Murcia Pienkowski VA; Department of Medical Genetics, Medical University of Warsaw, Warsaw, Poland.
  • Biernacka A; Department of Medical Genetics, Medical University of Warsaw, Warsaw, Poland.
  • Skiba P; Postgraduate School of Molecular Medicine, Medical University of Warsaw, Warsaw, Poland.
  • Machnik-Broncel J; Department of Medical Genetics, Medical University of Warsaw, Warsaw, Poland.
  • Gasperowicz P; Postgraduate School of Molecular Medicine, Medical University of Warsaw, Warsaw, Poland.
  • Kosinska J; Department of Genetics, Wroclaw Medical University, Wroclaw, Poland.
  • Rydzanicz M; Department of Diagnostic Imaging, Medical University of Silesia, Katowice, Poland.
  • Emich-Widera E; Department of Medical Genetics, Medical University of Warsaw, Warsaw, Poland.
  • Ploski R; Department of Medical Genetics, Medical University of Warsaw, Warsaw, Poland.
Clin Genet ; 94(3-4): 381-385, 2018 10.
Article en En | MEDLINE | ID: mdl-29938792
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Ribonucleoproteína Heterogénea-Nuclear Grupo F-H / Discapacidad Intelectual Límite: Adolescent / Female / Humans / Male Idioma: En Revista: Clin Genet Año: 2018 Tipo del documento: Article País de afiliación: Polonia Pais de publicación: Dinamarca
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Ribonucleoproteína Heterogénea-Nuclear Grupo F-H / Discapacidad Intelectual Límite: Adolescent / Female / Humans / Male Idioma: En Revista: Clin Genet Año: 2018 Tipo del documento: Article País de afiliación: Polonia Pais de publicación: Dinamarca