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Study of rare genetic variants in TM4SF20, NFXL1, CNTNAP2, and ATP2C2 in Pakistani probands and families with language impairment.
Andres, Erin M; Neely, Heather L; Hafeez, Huma; Yasmin, Tahira; Kausar, Farzana; Basra, M Asim Raza; Raza, Muhammad Hashim.
Afiliação
  • Andres EM; University of Kansas, Child Language Doctoral Program.
  • Neely HL; University of Kansas, Child Language Doctoral Program.
  • Hafeez H; School of Chemistry, University of the Punjab.
  • Yasmin T; School of Chemistry, University of the Punjab.
  • Kausar F; School of Chemistry, University of the Punjab.
  • Basra MAR; School of Chemistry, University of the Punjab.
  • Raza MH; University of Kansas, Child Language Doctoral Program.
Meta Gene ; 302021 Dec.
Article em En | MEDLINE | ID: mdl-34540591
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies Idioma: En Revista: Meta Gene Ano de publicação: 2021 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies Idioma: En Revista: Meta Gene Ano de publicação: 2021 Tipo de documento: Article