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PRRT2-related phenotypes in patients with a 16p11.2 deletion.
Vlaskamp, Danique R M; Callenbach, Petra M C; Rump, Patrick; Giannini, Lucia A A; Brilstra, Eva H; Dijkhuizen, Trijnie; Vos, Yvonne J; van der Kevie-Kersemaekers, Anne-Marie F; Knijnenburg, Jeroen; de Leeuw, Nicole; van Minkelen, Rick; Ruivenkamp, Claudia A L; Stegmann, Alexander P A; Brouwer, Oebele F; van Ravenswaaij-Arts, Conny M A.
Afiliação
  • Vlaskamp DRM; University of Groningen, University Medical Center Groningen, Department of Neurology, Groningen, The Netherlands; University of Groningen, University Medical Center Groningen, Department of Genetics, Groningen, The Netherlands.
  • Callenbach PMC; University of Groningen, University Medical Center Groningen, Department of Neurology, Groningen, The Netherlands.
  • Rump P; University of Groningen, University Medical Center Groningen, Department of Genetics, Groningen, The Netherlands.
  • Giannini LAA; University of Groningen, University Medical Center Groningen, Department of Genetics, Groningen, The Netherlands.
  • Brilstra EH; University Medical Center Utrecht, Department of Genetics, Utrecht, The Netherlands.
  • Dijkhuizen T; University of Groningen, University Medical Center Groningen, Department of Genetics, Groningen, The Netherlands.
  • Vos YJ; University of Groningen, University Medical Center Groningen, Department of Genetics, Groningen, The Netherlands.
  • van der Kevie-Kersemaekers AF; Academic Medical Center, Department of Genetics, Amsterdam, The Netherlands.
  • Knijnenburg J; Erasmus Medical Center, Department of Genetics, Rotterdam, The Netherlands.
  • de Leeuw N; Radboud University Medical Center, Department of Genetics, Nijmegen, The Netherlands.
  • van Minkelen R; Erasmus Medical Center, Department of Genetics, Rotterdam, The Netherlands.
  • Ruivenkamp CAL; Leiden University Medical Center, Department of Genetics, Leiden, The Netherlands.
  • Stegmann APA; Maastricht University Medical Center, Department of Genetics, Maastricht, The Netherlands.
  • Brouwer OF; University of Groningen, University Medical Center Groningen, Department of Neurology, Groningen, The Netherlands.
  • van Ravenswaaij-Arts CMA; University of Groningen, University Medical Center Groningen, Department of Genetics, Groningen, The Netherlands. Electronic address: c.m.a.van.ravenswaaij@umcg.nl.
Eur J Med Genet ; 62(4): 265-269, 2019 Apr.
Article em En | MEDLINE | ID: mdl-30125676
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fenótipo / Transtorno Autístico / Transtornos Cromossômicos / Proteínas de Membrana / Deficiência Intelectual / Proteínas do Tecido Nervoso Limite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Male Idioma: En Revista: Eur J Med Genet Assunto da revista: GENETICA MEDICA Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Holanda País de publicação: Holanda
Texto completo
Adicionar na Minha BVS
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XML
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Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fenótipo / Transtorno Autístico / Transtornos Cromossômicos / Proteínas de Membrana / Deficiência Intelectual / Proteínas do Tecido Nervoso Limite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Male Idioma: En Revista: Eur J Med Genet Assunto da revista: GENETICA MEDICA Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Holanda País de publicação: Holanda