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An eight-case 1q21 region series: novel aberrations and clinical variability with new features.
Ceylan, A C; Sahin, I; Erdem, H B; Kayhan, G; Simsek-Kiper, P O; Utine, G E; Percin, F; Boduroglu, K; Alikasifoglu, M.
Afiliación
  • Ceylan AC; Faculty of Medicine, Department of Medical Genetics, Hacettepe University, Ankara, Turkey.
  • Sahin I; Department of Medical Genetics, Ankara Ataturk Training and Research Hospital, Yildirim Beyazit University, Ankara, Turkey.
  • Erdem HB; Faculty of Medicine, Department of Medical Genetics, Ataturk University, Erzurum, Turkey.
  • Kayhan G; Department of Medical Genetics, Ankara Diskapi Yildirim Beyazit Training and Research Hospital, Ankara, Turkey.
  • Simsek-Kiper PO; Faculty of Medicine, Department of Medical Genetics, Ataturk University, Erzurum, Turkey.
  • Utine GE; Department of Medical Genetics, Ankara Diskapi Yildirim Beyazit Training and Research Hospital, Ankara, Turkey.
  • Percin F; Faculty of Medicine, Department of Medical Genetics, Gazi University, Ankara, Turkey.
  • Boduroglu K; Faculty of Medicine, Department of Pediatric Genetics, Hacettepe University, Ankara, Turkey.
  • Alikasifoglu M; Faculty of Medicine, Department of Pediatric Genetics, Hacettepe University, Ankara, Turkey.
J Intellect Disabil Res ; 63(6): 548-557, 2019 06.
Article en En | MEDLINE | ID: mdl-30773728
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Anomalías Múltiples / Cromosomas Humanos Par 1 / Deleción Cromosómica / Megalencefalia / Duplicación Cromosómica / Discapacidad Intelectual Tipo de estudio: Etiology_studies / Prognostic_studies Límite: Adolescent / Child / Child, preschool / Female / Humans / Infant / Male Idioma: En Revista: J Intellect Disabil Res Asunto de la revista: TRANSTORNOS MENTAIS Año: 2019 Tipo del documento: Article País de afiliación: Turquía Pais de publicación: Reino Unido
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Anomalías Múltiples / Cromosomas Humanos Par 1 / Deleción Cromosómica / Megalencefalia / Duplicación Cromosómica / Discapacidad Intelectual Tipo de estudio: Etiology_studies / Prognostic_studies Límite: Adolescent / Child / Child, preschool / Female / Humans / Infant / Male Idioma: En Revista: J Intellect Disabil Res Asunto de la revista: TRANSTORNOS MENTAIS Año: 2019 Tipo del documento: Article País de afiliación: Turquía Pais de publicación: Reino Unido