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Continuing role for classical cytogenetics: Case report of a boy with ring syndrome caused by complete ring chromosome 4 and review of literature.
Burgemeister, Anna Lena; Daumiller, Eva; Dietze-Armana, Ilona; Klett, Christine; Freiberg, Clemens; Stark, Wiebke; Lingen, Michael; Centonze, Izabela; Rettenberger, Günther; Mehnert, Karl; Zirn, Birgit.
Afiliación
  • Burgemeister AL; Genetikum, Genetic Counseling and Diagnostics, Stuttgart and Neu-Ulm, Germany.
  • Daumiller E; Genetikum, Genetic Counseling and Diagnostics, Stuttgart and Neu-Ulm, Germany.
  • Dietze-Armana I; Genetikum, Genetic Counseling and Diagnostics, Stuttgart and Neu-Ulm, Germany.
  • Klett C; Genetikum, Genetic Counseling and Diagnostics, Stuttgart and Neu-Ulm, Germany.
  • Freiberg C; Department of Pediatrics and Adolescent Medicine, Pediatric Endocrinology, University Medicine, Göttingen, Germany.
  • Stark W; Department of Pediatrics and Adolescent Medicine, Pediatric Neurology, University Medicine, Göttingen, Germany.
  • Lingen M; Department of Pediatrics and Adolescent Medicine, Pediatric Neurology, University Medicine, Göttingen, Germany.
  • Centonze I; Genetikum, Genetic Counseling and Diagnostics, Stuttgart and Neu-Ulm, Germany.
  • Rettenberger G; Genetikum, Genetic Counseling and Diagnostics, Stuttgart and Neu-Ulm, Germany.
  • Mehnert K; Genetikum, Genetic Counseling and Diagnostics, Stuttgart and Neu-Ulm, Germany.
  • Zirn B; Genetikum, Genetic Counseling and Diagnostics, Stuttgart and Neu-Ulm, Germany.
Am J Med Genet A ; 173(3): 727-732, 2017 Mar.
Article en En | MEDLINE | ID: mdl-28127864
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Trastornos de los Cromosomas / Análisis Citogenético Tipo de estudio: Prognostic_studies Límite: Child / Humans / Male Idioma: En Revista: Am J Med Genet A Asunto de la revista: GENETICA MEDICA Año: 2017 Tipo del documento: Article País de afiliación: Alemania
Texto completo
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Trastornos de los Cromosomas / Análisis Citogenético Tipo de estudio: Prognostic_studies Límite: Child / Humans / Male Idioma: En Revista: Am J Med Genet A Asunto de la revista: GENETICA MEDICA Año: 2017 Tipo del documento: Article País de afiliación: Alemania