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Interstitial 6q21q23 duplication - variant of variable phenotype and incomplete penetrance or benign duplication?
Srebniak, Malgorzata I; van Zutven, Laura J C M; Petit, Florence; Bouquillon, Sonia; van Heel, Ilse P J; Knapen, Maarten F C M; Cornette, Jerome M J; Kremer, Andreas; Van Opstal, Diane; Diderich, Karin E M.
Afiliação
  • Srebniak MI; Department of Clinical Genetics, Erasmus MC, Ee2475, Wytemaweg 80, 3015 CN Rotterdam, The Netherlands.
  • van Zutven LJ; Department of Clinical Genetics, Erasmus MC, Ee2475, Wytemaweg 80, 3015 CN Rotterdam, The Netherlands.
  • Petit F; Department of Clinical Genetics, University Hospital, Lille, France.
  • Bouquillon S; Department of Cytogenetics, University Hospital, Lille, France.
  • van Heel IP; Department of Clinical Genetics, Erasmus MC, Ee2475, Wytemaweg 80, 3015 CN Rotterdam, The Netherlands.
  • Knapen MF; Department of Obstetrics and Gynecology, subdivision Obstetrics and Prenatal Medicine, Erasmus MC, Rotterdam, The Netherlands ; Stichting Prenatale Screening Zuidwest Nederland, Wytemaweg 80, Na-1509, 3015, GE Na-1503 Rotterdam, The Netherlands.
  • Cornette JM; Department of Obstetrics and Gynecology, subdivision Obstetrics and Prenatal Medicine, Erasmus MC, Rotterdam, The Netherlands.
  • Kremer A; Department of Bioinformatics Erasmus MC, Rotterdam, The Netherlands.
  • Van Opstal D; Department of Clinical Genetics, Erasmus MC, Ee2475, Wytemaweg 80, 3015 CN Rotterdam, The Netherlands.
  • Diderich KE; Department of Clinical Genetics, Erasmus MC, Ee2475, Wytemaweg 80, 3015 CN Rotterdam, The Netherlands.
Mol Cytogenet ; 9: 43, 2016.
Article em En | MEDLINE | ID: mdl-27274769
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2016 Tipo de documento: Article País de afiliação: Holanda
Texto completo
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XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2016 Tipo de documento: Article País de afiliação: Holanda