T. Jamil

Truncation of the E3 ubiquitin ligase component FBXO31 causes non-syndromic autosomal recessive intellectual disability in a Pakistani family

J. Vincent, M. Rafiq, J. So, 2014, Human Genetics.

Haplotype Analysis for DFNB4/PDS Locus in Hearing Impaired Families of Punjab (Pakistan)

J. Khattak, A. Mir, S. B. Jamal, 2012 .

Phosphoserine phosphatase (PSPH) gene mutation in an intellectual disability family from Pakistan

J. Vincent, M. Rafiq, E. Schaftingen, 2015, Clinical genetics.

Truncation of the E3 ubiquitin ligase component FBXO31 causes non-syndromic autosomal recessive intellectual disability in a Pakistani family

J. Vincent, M. Rafiq, J. So, 2014, Human Genetics.

Identification of mutations in TRAPPC9, which encodes the NIK- and IKK-beta-binding protein, in nonsyndromic autosomal-recessive mental retardation.

A. Noor, J. Vincent, R. Weksberg, 2009, American journal of human genetics.