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A review of structural brain abnormalities in Pallister-Killian syndrome.
Poulton, Cathryn; Baynam, Gareth; Yates, Clarissa; Alinejad-Rokny, Hamid; Williams, Simon; Wright, Helen; Woodward, Karen J; Sivamoorthy, Soruba; Peverall, Joanne; Shipman, Peter; Ravine, David; Beilby, John; Heng, Julian Ik-Tsen.
Afiliação
  • Poulton C; Department of Neurology, Princess Margaret Hospital, Subiaco, WA, Australia.
  • Baynam G; Telethon Kids Institute, University of Western Australia, Perth, WA, Australia.
  • Yates C; Genetic Services of Western Australia, Perth, WA, Australia.
  • Alinejad-Rokny H; Office of Population Health Genomics, Public Health and Clinical Services Division, Department of Health, Government of Western Australia, Perth, WA, Australia.
  • Williams S; School of Paediatrics and Child Health, University of Western Australia, Perth, WA, Australia.
  • Wright H; Institute for Immunology and Infectious Diseases, Murdoch University, Perth, WA, Australia.
  • Woodward KJ; Western Australian Register of Developmental Anomalies, Perth, WA, Australia.
  • Sivamoorthy S; Spatial Sciences, Science and Engineering, Curtin University, Crawley, WA, Australia.
  • Peverall J; Centre for Medical Research, the University of Western Australia, Nedlands, WA, Australia.
  • Shipman P; Centre for Medical Research, the University of Western Australia, Nedlands, WA, Australia.
  • Ravine D; The Harry Perkins Institute of Medical Research, QEII Medical Centre, Nedlands, WA, Australia.
  • Beilby J; Department of Neurology, Princess Margaret Hospital, Subiaco, WA, Australia.
  • Heng JI; Department of Paediatrics, Princess Margaret Hospital, Subiaco, WA, Australia.
Mol Genet Genomic Med ; 6(1): 92-98, 2018 01.
Article em En | MEDLINE | ID: mdl-29222831
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Encéfalo / Transtornos Cromossômicos Tipo de estudo: Prognostic_studies Limite: Child, preschool / Humans / Male Idioma: En Revista: Mol Genet Genomic Med Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Austrália
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Encéfalo / Transtornos Cromossômicos Tipo de estudo: Prognostic_studies Limite: Child, preschool / Humans / Male Idioma: En Revista: Mol Genet Genomic Med Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Austrália