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Variable developmental delays and characteristic facial features-A novel 7p22.3p22.2 microdeletion syndrome?
Yu, Andrea C; Zambrano, Regina M; Cristian, Ingrid; Price, Sue; Bernhard, Birgitta; Zucker, Marc; Venkateswaran, Sunita; McGowan-Jordan, Jean; Armour, Christine M.
Afiliação
  • Yu AC; Department of Genetics, Children's Hospital of Eastern Ontario, Ottawa, Ontario, Canada.
  • Zambrano RM; Division of Clinical Genetics, Department of Pediatrics, Louisiana State University Health Science Center, New Orleans, Louisiana.
  • Cristian I; Division of Genetics and Metabolism, Department of Pediatrics, Nemours Children's Hospital Orlando, Orlando, Florida.
  • Price S; Oxford Regional Genetic Service, Churchill Hospital, Oxford, UK.
  • Bernhard B; North West Thames Regional Genetic Service, North West London Hospitals, Greater London, England.
  • Zucker M; Department of Pediatrics, Children's Hospital of Eastern Ontario, Ottawa, Ontario, Canada.
  • Venkateswaran S; Division of Neurology, Children's Hospital of Eastern Ontario, Ottawa, Ontario, Canada.
  • McGowan-Jordan J; Department of Pathology and Laboratory Medicine, University of Ottawa, Ottawa, Ontario, Canada.
  • Armour CM; Department of Genetics, Children's Hospital of Eastern Ontario, Ottawa, Ontario, Canada.
Am J Med Genet A ; 173(6): 1593-1600, 2017 Jun.
Article em En | MEDLINE | ID: mdl-28440577

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Cromossomos Humanos Par 7 / Deficiências do Desenvolvimento / Deleção Cromossômica Limite: Child, preschool / Female / Humans / Infant / Male Idioma: En Revista: Am J Med Genet A Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Cromossomos Humanos Par 7 / Deficiências do Desenvolvimento / Deleção Cromossômica Limite: Child, preschool / Female / Humans / Infant / Male Idioma: En Revista: Am J Med Genet A Ano de publicação: 2017 Tipo de documento: Article