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Cardiovascular malformations caused by NOTCH1 mutations do not keep left: data on 428 probands with left-sided CHD and their families.
Kerstjens-Frederikse, Wilhelmina S; van de Laar, Ingrid M B H; Vos, Yvonne J; Verhagen, Judith M A; Berger, Rolf M F; Lichtenbelt, Klaske D; Klein Wassink-Ruiter, Jolien S; van der Zwaag, Paul A; du Marchie Sarvaas, Gideon J; Bergman, Klasien A; Bilardo, Catia M; Roos-Hesselink, Jolien W; Janssen, Johan H P; Frohn-Mulder, Ingrid M; van Spaendonck-Zwarts, Karin Y; van Melle, Joost P; Hofstra, Robert M W; Wessels, M W.
Afiliación
  • Kerstjens-Frederikse WS; Department of Genetics, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands.
  • van de Laar IM; Department of Clinical Genetics, Erasmus Medical Center, Rotterdam, The Netherlands.
  • Vos YJ; Department of Genetics, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands.
  • Verhagen JM; Department of Clinical Genetics, Erasmus Medical Center, Rotterdam, The Netherlands.
  • Berger RM; Center for Congenital Heart Diseases, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands.
  • Lichtenbelt KD; Department of Genetics, University Medical Center Utrecht, Utrecht, The Netherlands.
  • Klein Wassink-Ruiter JS; Department of Genetics, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands.
  • van der Zwaag PA; Department of Genetics, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands.
  • du Marchie Sarvaas GJ; Center for Congenital Heart Diseases, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands.
  • Bergman KA; Department of Pediatrics, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands.
  • Bilardo CM; Department of Obstetrics and Gynaecology, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands.
  • Roos-Hesselink JW; Department of Cardiology, Erasmus Medical Center, Rotterdam, The Netherlands.
  • Janssen JH; Department of Cardiology, Saint Anna Hospital, Geldrop, The Netherlands.
  • Frohn-Mulder IM; Department of Pediatric Cardiology, Erasmus Medical Center, Rotterdam, The Netherlands.
  • van Spaendonck-Zwarts KY; Department of Genetics, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands.
  • van Melle JP; Center for Congenital Heart Diseases, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands.
  • Hofstra RM; Department of Genetics, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands.
  • Wessels MW; Department of Clinical Genetics, Erasmus Medical Center, Rotterdam, The Netherlands.
Genet Med ; 18(9): 914-23, 2016 09.
Article en En | MEDLINE | ID: mdl-26820064
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Síndrome del Corazón Izquierdo Hipoplásico / Receptor Notch1 / Cardiopatías Congénitas / Insuficiencia Cardíaca Tipo de estudio: Prognostic_studies / Risk_factors_studies / Screening_studies Límite: Adolescent / Adult / Aged / Child / Child, preschool / Female / Humans / Male / Middle aged Idioma: En Revista: Genet Med Asunto de la revista: GENETICA MEDICA Año: 2016 Tipo del documento: Article País de afiliación: Países Bajos
Texto completo
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Síndrome del Corazón Izquierdo Hipoplásico / Receptor Notch1 / Cardiopatías Congénitas / Insuficiencia Cardíaca Tipo de estudio: Prognostic_studies / Risk_factors_studies / Screening_studies Límite: Adolescent / Adult / Aged / Child / Child, preschool / Female / Humans / Male / Middle aged Idioma: En Revista: Genet Med Asunto de la revista: GENETICA MEDICA Año: 2016 Tipo del documento: Article País de afiliación: Países Bajos