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Fragile X syndrome with mosaic size mutation in a Bantu patient from Central Africa.
Lubala, Toni K; Lumaka, Aimé; Mbuyi-Musanzayi, Sébastien; Kayembe, Tony; Shongo, Mick Y P; Mukuku, Olivier; Lubala, Nina; Malamba-Lez, Didier; Luboya, Oscar N; Lukusa-Tshilobo, Prosper.
Afiliación
  • Lubala TK; Department of Pediatrics, Faculty of Medicine, University of Lubumbashi.
  • Lumaka A; Department of Pediatrics, University Hospitals.
  • Mbuyi-Musanzayi S; Centre for Human Genetics, Faculty of Medicine, University of Kinshasa, Kinshasa, Democratic Republic of the Congo.
  • Kayembe T; Department of Human Genetics, University Hospitals, University of Leuven, KU Leuven, Leuven, Belgium.
  • Shongo MYP; Department of Surgery.
  • Mukuku O; Department of Pediatrics, Faculty of Medicine, University of Lubumbashi.
  • Lubala N; Department of Pediatrics, Faculty of Medicine, University of Lubumbashi.
  • Malamba-Lez D; Department of Pediatrics, Faculty of Medicine, University of Lubumbashi.
  • Luboya ON; Department of Specialities.
  • Lukusa-Tshilobo P; Department of Internal Medicine, Division of Cardiology, University Hospital, University of Lubumbashi, Lubumbashi.
Clin Dysmorphol ; 27(2): 66-69, 2018 Apr.
Article en En | MEDLINE | ID: mdl-29319541
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Proteína de la Discapacidad Intelectual del Síndrome del Cromosoma X Frágil / Síndrome del Cromosoma X Frágil Límite: Adolescent / Humans / Male País/Región como asunto: Africa Idioma: En Revista: Clin Dysmorphol Asunto de la revista: TERATOLOGIA Año: 2018 Tipo del documento: Article
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Proteína de la Discapacidad Intelectual del Síndrome del Cromosoma X Frágil / Síndrome del Cromosoma X Frágil Límite: Adolescent / Humans / Male País/Región como asunto: Africa Idioma: En Revista: Clin Dysmorphol Asunto de la revista: TERATOLOGIA Año: 2018 Tipo del documento: Article