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Clinical and molecular characterization of an infant with a tandem duplication and deletion of 19p13.
Tan, Ratna N G B; Witlox, Ruben S G M; Hilhorst-Hofstee, Yvonne; Peeters-Scholte, Cacha M P C D; den Hollander, Nicolette S; Ruivenkamp, Claudia A L; Hoffer, Mariëtte J V; Hansson, Kerstin B; van Roosmalen, Mark J; Kloosterman, Wigard P; Santen, Gijs W E.
Afiliação
  • Tan RN; Department of Pediatrics, Leiden University Medical Center, Leiden, the Netherlands.
  • Witlox RS; Department of Pediatrics, Leiden University Medical Center, Leiden, the Netherlands.
  • Hilhorst-Hofstee Y; Department of Clinical Genetics, Leiden University Medical Center, Leiden, the Netherlands.
  • Peeters-Scholte CM; Department of Neurology, Leiden University Medical Center, Leiden, the Netherlands.
  • den Hollander NS; Department of Clinical Genetics, Leiden University Medical Center, Leiden, the Netherlands.
  • Ruivenkamp CA; Department of Clinical Genetics, Leiden University Medical Center, Leiden, the Netherlands.
  • Hoffer MJ; Department of Clinical Genetics, Leiden University Medical Center, Leiden, the Netherlands.
  • Hansson KB; Department of Clinical Genetics, Leiden University Medical Center, Leiden, the Netherlands.
  • van Roosmalen MJ; Center for Molecular Medicine, Department of Medical Genetics, University Medical Center Utrecht, Utrecht, the Netherlands.
  • Kloosterman WP; Center for Molecular Medicine, Department of Medical Genetics, University Medical Center Utrecht, Utrecht, the Netherlands.
  • Santen GW; Department of Clinical Genetics, Leiden University Medical Center, Leiden, the Netherlands.
Am J Med Genet A ; 167A(8): 1884-9, 2015 Aug.
Article em En | MEDLINE | ID: mdl-25900458
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Cromossomos Humanos Par 19 / Deleção Cromossômica / Duplicação Cromossômica Limite: Humans / Male / Newborn Idioma: En Revista: Am J Med Genet A Assunto da revista: GENETICA MEDICA Ano de publicação: 2015 Tipo de documento: Article País de afiliação: Holanda País de publicação: Estados Unidos
Texto completo
Adicionar na Minha BVS
Imprimir
XML
PubMed Links
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Cromossomos Humanos Par 19 / Deleção Cromossômica / Duplicação Cromossômica Limite: Humans / Male / Newborn Idioma: En Revista: Am J Med Genet A Assunto da revista: GENETICA MEDICA Ano de publicação: 2015 Tipo de documento: Article País de afiliação: Holanda País de publicação: Estados Unidos