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A 9.8 Mb deletion at 7q31.2q31.31 downstream of FOXP2 in an individual with speech and language impairment suggests a possible positional effect.
Iwata-Otsubo, Aiko; Klee, Victoria H; Ahmad, Aaliya A; Walsh, Laurence E; Breman, Amy M.
Afiliação
  • Iwata-Otsubo A; Department of Medical and Molecular Genetics Indiana University School of Medicine Indianapolis Indiana USA.
  • Klee VH; Department of Neurology, Section of Child Neurology Indiana University School of Medicine Indianapolis Indiana USA.
  • Ahmad AA; Department of Medical and Molecular Genetics Indiana University School of Medicine Indianapolis Indiana USA.
  • Walsh LE; Department of Medical and Molecular Genetics Indiana University School of Medicine Indianapolis Indiana USA.
  • Breman AM; Department of Neurology, Section of Child Neurology Indiana University School of Medicine Indianapolis Indiana USA.
Clin Case Rep ; 10(11): e6535, 2022 Nov.
Article em En | MEDLINE | ID: mdl-36415709

Texto completo: 1 Base de dados: MEDLINE Idioma: En Revista: Clin Case Rep Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Revista: Clin Case Rep Ano de publicação: 2022 Tipo de documento: Article