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Genotype and brain pathology phenotype in children with tuberous sclerosis complex.
Overwater, Iris E; Swenker, Rob; van der Ende, Emma L; Hanemaayer, Kimberley Bm; Hoogeveen-Westerveld, Marianne; van Eeghen, Agnies M; Lequin, Maarten H; van den Ouweland, Ans Mw; Moll, Henriëtte A; Nellist, Mark; de Wit, Marie-Claire Y.
Afiliação
  • Overwater IE; Department of Neurology, Erasmus Medical Center, Rotterdam, The Netherlands.
  • Swenker R; ENCORE-TSC Expertise Center, Erasmus Medical Center, Rotterdam, The Netherlands.
  • van der Ende EL; Department of Clinical Genetics, Erasmus Medical Center, Rotterdam, The Netherlands.
  • Hanemaayer KB; Department of Neurology, Erasmus Medical Center, Rotterdam, The Netherlands.
  • Hoogeveen-Westerveld M; Department of Neurology, Erasmus Medical Center, Rotterdam, The Netherlands.
  • van Eeghen AM; Department of Clinical Genetics, Erasmus Medical Center, Rotterdam, The Netherlands.
  • Lequin MH; ENCORE-TSC Expertise Center, Erasmus Medical Center, Rotterdam, The Netherlands.
  • van den Ouweland AM; Department of Pediatrics, Erasmus Medical Center, Rotterdam, The Netherlands.
  • Moll HA; Department of Radiology, University Medical Centre Utrecht, Utrecht, The Netherlands.
  • Nellist M; Department of Clinical Genetics, Erasmus Medical Center, Rotterdam, The Netherlands.
  • de Wit MY; ENCORE-TSC Expertise Center, Erasmus Medical Center, Rotterdam, The Netherlands.
Eur J Hum Genet ; 24(12): 1688-1695, 2016 12.
Article em En | MEDLINE | ID: mdl-27406250
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fenótipo / Esclerose Tuberosa / Encéfalo / Genótipo Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Adolescent / Child / Child, preschool / Female / Humans / Infant / Male Idioma: En Revista: Eur J Hum Genet Assunto da revista: GENETICA MEDICA Ano de publicação: 2016 Tipo de documento: Article País de afiliação: Holanda
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fenótipo / Esclerose Tuberosa / Encéfalo / Genótipo Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Adolescent / Child / Child, preschool / Female / Humans / Infant / Male Idioma: En Revista: Eur J Hum Genet Assunto da revista: GENETICA MEDICA Ano de publicação: 2016 Tipo de documento: Article País de afiliação: Holanda