Torthaí cuardaigh - Muhammad Hashim Raza

  • 1 - 3 toradh as 3 á dtaispeáint
Beachtaigh na torthaí
  1. 1
    Identification of an autosomal recessive stuttering locus on chromosome 3q13.2–3q13.33

    Identification of an autosomal recessive stuttering locus on chromosome 3q13.2–3q13.33 de réir Muhammad Hashim Raza, Sheikh Riazuddin, Dennis Drayna

    Foilsithe / Cruthaithe 2010
    Faigh an téacs iomlán
    Artigo
    Cuir le mo chuid Ceanán
    Sábháilte in:
  2. 2
    Association between Rare Variants in AP4E1, a Component of Intracellular Trafficking, and Persistent Stuttering

    Association between Rare Variants in AP4E1, a Component of Intracellular Trafficking, and Persistent Stuttering de réir Muhammad Hashim Raza, Rafael Mattera, Robert J. Morell, Eduardo Sainz, Rachel M. Rahn, Joanne Gutierrez, Emily Paris, Jessica Root, Beth Solomon, Carmen C. Brewer, Muhammad Asim Raza Basra, Shaheen Khan, Sheikh Riazuddin, Allen Braun, Juan S. Bonifacino, Dennis Drayna

    Foilsithe / Cruthaithe 2015
    Faigh an téacs iomlán
    Artigo
    Cuir le mo chuid Ceanán
    Sábháilte in:
  3. 3
    Mucolipidosis types II and III and non-syndromic stuttering are associated with different variants in the same genes

    Mucolipidosis types II and III and non-syndromic stuttering are associated with different variants in the same genes de réir Muhammad Hashim Raza, Carlos Eduardo Frigério Domingues, Ronald L. Webster, Eduardo Sainz, Emily Paris, Rachel M. Rahn, Joanne Gutierrez, Ho Ming Chow, Jennifer Mundorff, Chang-Soo Kang, Naveeda Riaz, Muhammad Asim Raza Basra, Shaheen Khan, Sheikh Riazuddin, Danilo Moretti‐Ferreira, Allen Braun, Dennis Drayna

    Foilsithe / Cruthaithe 2015
    Faigh an téacs iomlán Faigh an téacs iomlán
    Artigo
    Cuir le mo chuid Ceanán
    Sábháilte in:

Uirlisí cuardaigh: