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Prenatal Evidence of Persistent Notochord and Absent Sacrum Caused by a Mutation in the T (Brachyury) Gene.
Fontanella, F; van Maarle, M C; Robles de Medina, P; Oostra, R J; van Rijn, R R; Pajkrt, E; Bilardo, C M.
Afiliación
  • Fontanella F; Department of Obstetrics, Gynaecology and Prenatal Diagnosis, University Medical Center Groningen, University of Groningen, Groningen, Netherlands.
  • van Maarle MC; Department of Clinical Genetics, Academic Medical Center Amsterdam, Amsterdam, Netherlands.
  • Robles de Medina P; Department of Obstetrics and Gynaecology, Academic Medical Center Amsterdam, Amsterdam, Netherlands.
  • Oostra RJ; Department of Anatomy and Embryology, Academic Medical Center Amsterdam, Amsterdam, Netherlands.
  • van Rijn RR; Department of Radiology, Academic Medical Center Amsterdam, Amsterdam, Netherlands.
  • Pajkrt E; Department of Obstetrics and Gynaecology, Academic Medical Center Amsterdam, Amsterdam, Netherlands.
  • Bilardo CM; Department of Obstetrics, Gynaecology and Prenatal Diagnosis, University Medical Center Groningen, University of Groningen, Groningen, Netherlands.
Case Rep Obstet Gynecol ; 2016: 7625341, 2016.
Article en En | MEDLINE | ID: mdl-28116192
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Texto completo: 1 Banco de datos: MEDLINE Idioma: En Revista: Case Rep Obstet Gynecol Año: 2016 Tipo del documento: Article País de afiliación: Países Bajos
Texto completo
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Banco de datos: MEDLINE Idioma: En Revista: Case Rep Obstet Gynecol Año: 2016 Tipo del documento: Article País de afiliación: Países Bajos