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Blake's pouch cyst in 13q deletion syndrome: Posterior fossa malformations may occur due to disruption of multiple genes.
Myers, Kenneth A; Wallis, Mathew J; Fitt, Gregory J; Sarnat, Harvey B; Newton, Mark R.
Afiliação
  • Myers KA; Department of Neurology, University of Melbourne, Austin Health, Heidelberg, Australia.
  • Wallis MJ; Department of Clinical Genetics, University of Melbourne, Austin Health, Heidelberg, Australia.
  • Fitt GJ; Department of Radiology, University of Melbourne, Austin Health, Heidelberg, Australia.
  • Sarnat HB; Department of Paediatrics, Section of Neurology, University of Calgary Cumming School of Medicine, Alberta Children's Hospital, Calgary, Alberta, Canada.
  • Newton MR; Department of Neurology, University of Melbourne, Austin Health, Heidelberg, Australia.
Am J Med Genet A ; 173(9): 2442-2445, 2017 Sep.
Article em En | MEDLINE | ID: mdl-28686337
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fenótipo / Transtornos Cromossômicos Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Humans Idioma: En Ano de publicação: 2017 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fenótipo / Transtornos Cromossômicos Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Humans Idioma: En Ano de publicação: 2017 Tipo de documento: Article