Your browser doesn't support javascript.
loading
Schizencephaly accompanied by occipital encephalocele and deletion of chromosome 22q13.32: a case report.
Inan, Cihan; Sayin, N Cenk; Gurkan, Hakan; Atli, Engin; Gursoy Erzincan, Selen; Uzun, Isil; Sutcu, Havva; Dogan, Sumeyra; Ikbal Atli, Emine; Varol, Fusun.
Afiliación
  • Inan C; Division of Perinatology, Department of Obstetrics & Gynecology, Faculty of Medicine, Trakya University, Edirne, Turkey.
  • Sayin NC; Division of Perinatology, Department of Obstetrics & Gynecology, Faculty of Medicine, Trakya University, Edirne, Turkey.
  • Gurkan H; Department of Medical Genetics, Faculty of Medicine, Trakya University, Edirne, Turkey.
  • Atli E; Department of Medical Genetics, Faculty of Medicine, Trakya University, Edirne, Turkey.
  • Gursoy Erzincan S; Division of Perinatology, Department of Obstetrics & Gynecology, Faculty of Medicine, Trakya University, Edirne, Turkey.
  • Uzun I; Division of Perinatology, Department of Obstetrics & Gynecology, Faculty of Medicine, Trakya University, Edirne, Turkey.
  • Sutcu H; Division of Perinatology, Department of Obstetrics & Gynecology, Faculty of Medicine, Trakya University, Edirne, Turkey.
  • Dogan S; Department of Radiology, Faculty of Medicine, Trakya University, Edirne, Turkey.
  • Ikbal Atli E; Department of Medical Genetics, Faculty of Medicine, Trakya University, Edirne, Turkey.
  • Varol F; Division of Perinatology, Department of Obstetrics & Gynecology, Faculty of Medicine, Trakya University, Edirne, Turkey.
Fetal Pediatr Pathol ; 38(6): 496-502, 2019 Dec.
Article en En | MEDLINE | ID: mdl-31130048
Asunto(s)
Palabras clave
Texto completo
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Anomalías Múltiples / Cromosomas Humanos Par 22 / Deleción Cromosómica / Encefalocele / Esquizencefalia Tipo de estudio: Diagnostic_studies Límite: Adult / Female / Humans Idioma: En Revista: Fetal Pediatr Pathol Asunto de la revista: PATOLOGIA / PEDIATRIA Año: 2019 Tipo del documento: Article País de afiliación: Turquía
Texto completo
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Anomalías Múltiples / Cromosomas Humanos Par 22 / Deleción Cromosómica / Encefalocele / Esquizencefalia Tipo de estudio: Diagnostic_studies Límite: Adult / Female / Humans Idioma: En Revista: Fetal Pediatr Pathol Asunto de la revista: PATOLOGIA / PEDIATRIA Año: 2019 Tipo del documento: Article País de afiliación: Turquía