Search filters

List of works by Muhammad Ansar

A novel WDR62 mutation causes primary microcephaly in a Pakistani family

scientific article published on 14 October 2012

A novel autosomal recessive non-syndromic hearing impairment locus (DFNB47) maps to chromosome 2p25.1-p24.3.

scientific article

A novel autosomal recessive nonsyndromic hearing impairment locus (DFNB42) maps to chromosome 3q13.31-q22.3.

scientific article published in February 2005

A novel pathogenic missense variant in CNNM4 underlying Jalili syndrome: Insights from molecular dynamics simulations

scientific article published on 25 July 2019

A recurrent intragenic deletion mutation in DSG4 gene in three Pakistani families with autosomal recessive hypotrichosis

scientific article

DFNB39, a recessive form of sensorineural hearing impairment, maps to chromosome 7q11.22-q21.12.

scientific article

Genetic studies of autosomal recessive primary microcephaly in 33 Pakistani families: Novel sequence variants in ASPM gene.

scientific article published on 21 April 2006

Intragenic deletions in the dystrophin gene in 211 Pakistani Duchenne muscular dystrophy patients.

scientific article

Novel autosomal recessive non-syndromic hearing impairment locus (DFNB71) maps to chromosome 8p22-21.3.

scientific article published on 20 February 2009

Recurrent intragenic deletion mutation in desmoglein 4 gene underlies autosomal recessive hypotrichosis in two Pakistani families of Balochi and Sindhi origins

scientific article published on 13 June 2006

Recurrent mutations in functionally-related EDA and EDAR genes underlie X-linked isolated hypodontia and autosomal recessive hypohidrotic ectodermal dysplasia

scientific article published on 24 June 2009

Paulina is supported by:

About Paulina

Help