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Phenotypic and molecular insights into PQBP1-related intellectual disability.
Abdel-Salam, Ghada M H; Miyake, Noriko; Abdel-Hamid, Mohamed S; Sayed, Inas S M; Gadelhak, Mohamed I; Ismail, Samira I; Aglan, Mona S; Afifi, Hanan H; Temtamy, Samia A; Matsumoto, Naomichi.
Afiliación
  • Abdel-Salam GMH; Clinical Genetics Department, Human Genetics and Genome Research Division, National Research Centre, Cairo, Egypt.
  • Miyake N; Department of Human Genetics, Yokohama City University Graduate School of Medicine, Yokohama, Japan.
  • Abdel-Hamid MS; Medical Molecular Genetics Department, Human Genetics and Genome Research Division, National Research Centre, Cairo, Egypt.
  • Sayed ISM; Orodental Genetics Department, Human Genetics and Genome Research Division, National Research Centre, Cairo, Egypt.
  • Gadelhak MI; Clinical Genetics Department, Human Genetics and Genome Research Division, National Research Centre, Cairo, Egypt.
  • Ismail SI; Clinical Genetics Department, Human Genetics and Genome Research Division, National Research Centre, Cairo, Egypt.
  • Aglan MS; Clinical Genetics Department, Human Genetics and Genome Research Division, National Research Centre, Cairo, Egypt.
  • Afifi HH; Clinical Genetics Department, Human Genetics and Genome Research Division, National Research Centre, Cairo, Egypt.
  • Temtamy SA; Clinical Genetics Department, Human Genetics and Genome Research Division, National Research Centre, Cairo, Egypt.
  • Matsumoto N; Department of Human Genetics, Yokohama City University Graduate School of Medicine, Yokohama, Japan.
Am J Med Genet A ; 176(11): 2446-2450, 2018 11.
Article en En | MEDLINE | ID: mdl-30244542
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Proteínas Nucleares / Proteínas Portadoras / Discapacidad Intelectual Tipo de estudio: Prognostic_studies Límite: Adult / Child / Child, preschool / Humans / Infant / Male / Newborn Idioma: En Revista: Am J Med Genet A Asunto de la revista: GENETICA MEDICA Año: 2018 Tipo del documento: Article País de afiliación: Egipto Pais de publicación: Estados Unidos
Texto completo
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Proteínas Nucleares / Proteínas Portadoras / Discapacidad Intelectual Tipo de estudio: Prognostic_studies Límite: Adult / Child / Child, preschool / Humans / Infant / Male / Newborn Idioma: En Revista: Am J Med Genet A Asunto de la revista: GENETICA MEDICA Año: 2018 Tipo del documento: Article País de afiliación: Egipto Pais de publicación: Estados Unidos