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Familial recurrences of FOXG1-related disorder: Evidence for mosaicism.
McMahon, Kelly Q; Papandreou, Apostolos; Ma, Mandy; Barry, Brenda J; Mirzaa, Ghayda M; Dobyns, William B; Scott, Richard H; Trump, Natalie; Kurian, Manju A; Paciorkowski, Alex R.
Afiliação
  • McMahon KQ; Department of Neurology, University of Rochester Medical Center, Rochester, New York.
  • Papandreou A; Developmental Neurosciences, UCL-Institute of Child Health, London, United Kingdom.
  • Ma M; Department of Neurology, Great Ormond Street Hospital, London, United Kingdom.
  • Barry BJ; Genetics and Genomics Medicine, UCL-Institute of Child Health, London, United Kingdom.
  • Mirzaa GM; University of Buffalo School of Medicine, Buffalo, New York.
  • Dobyns WB; Children's Hospital Boston, Boston, Massachusetts.
  • Scott RH; Department of Pediatrics, Division of Genetic Medicine, University of Washington, Center for Integrative Brain Research, Seattle Children's Research Institute, Seattle, Washington.
  • Trump N; Department of Pediatrics, Division of Genetic Medicine, University of Washington, Center for Integrative Brain Research, Seattle Children's Research Institute, Seattle, Washington.
  • Kurian MA; Genetics and Genomics Medicine, UCL-Institute of Child Health, London, United Kingdom.
  • Paciorkowski AR; North East Thames Regional Genetics Service, Great Ormond Street Hospital, London, United Kingdom.
Am J Med Genet A ; 167A(12): 3096-102, 2015 Dec.
Article em En | MEDLINE | ID: mdl-26364767
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fatores de Transcrição Forkhead / Mosaicismo / Mutação / Proteínas do Tecido Nervoso Tipo de estudo: Prognostic_studies Limite: Adolescent / Adult / Child / Female / Humans / Male Idioma: En Revista: Am J Med Genet A Ano de publicação: 2015 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: Fatores de Transcrição Forkhead / Mosaicismo / Mutação / Proteínas do Tecido Nervoso Tipo de estudo: Prognostic_studies Limite: Adolescent / Adult / Child / Female / Humans / Male Idioma: En Revista: Am J Med Genet A Ano de publicação: 2015 Tipo de documento: Article