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Variable neurodevelopmental and morphological phenotypes of carriers with 12q12 duplications.
Myers, Lynnea; Blyth, Moira; Moradkhani, Kamran; Hranilovic, Dubravka; Polesie, Sam; Isaksson, Johan; Nordgren, Ann; Bucan, Maja; Vincent, Marie; Bölte, Sven; Anderlid, Britt-Marie; Tammimies, Kristiina.
Afiliação
  • Myers L; Center of Neurodevelopmental Disorders (KIND), Centre for Psychiatry Research, Department of Women's and Children's Health, Karolinska Institutet & Child and Adolescent Psychiatry, Stockholm Health Care Services, Stockholm County Council, Stockholm, Sweden.
  • Blyth M; Department of Clinical Genetics, Chapel Allerton Hospital, Leeds, UK.
  • Moradkhani K; CHU Nantes, Service de Génétique Médicale, Nantes, France.
  • Hranilovic D; Department of Biology, Faculty of Science, University of Zagreb, Zagreb, Croatia.
  • Polesie S; Department of Dermatology and Venereology, Institute of Clinical Sciences, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.
  • Isaksson J; Department of Dermatology and Venereology, Region Västra Götaland, Sahlgrenska University Hospital, Gothenburg, Sweden.
  • Nordgren A; Center of Neurodevelopmental Disorders (KIND), Centre for Psychiatry Research, Department of Women's and Children's Health, Karolinska Institutet & Child and Adolescent Psychiatry, Stockholm Health Care Services, Stockholm County Council, Stockholm, Sweden.
  • Bucan M; Department of Neuroscience, Child and Adolescent Psychiatry and Psychiatry Unit, Uppsala University, Uppsala, Sweden.
  • Vincent M; Department of Molecular Medicine and Surgery, Karolinska Institutet, Stockholm, Sweden.
  • Bölte S; Department of Clinical Genetics, Karolinska University Hospital, Stockholm, Sweden.
  • Anderlid BM; Department of Genetics and Psychiatry, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.
  • Tammimies K; Centre Hospitalier, University of Nantes, Nantes, France.
Mol Genet Genomic Med ; 8(1): e1013, 2020 01.
Article em En | MEDLINE | ID: mdl-31730283
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fenótipo / Anormalidades Múltiplas / Cromossomos Humanos Par 12 / Deficiências do Desenvolvimento / Duplicação Cromossômica / Transtorno do Espectro Autista Limite: Humans / Infant / Male Idioma: En Revista: Mol Genet Genomic Med Ano de publicação: 2020 Tipo de documento: Article
Texto completo
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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 / Anormalidades Múltiplas / Cromossomos Humanos Par 12 / Deficiências do Desenvolvimento / Duplicação Cromossômica / Transtorno do Espectro Autista Limite: Humans / Infant / Male Idioma: En Revista: Mol Genet Genomic Med Ano de publicação: 2020 Tipo de documento: Article