S. K. Naqvi

Novel mutations in the keratin-74 (KRT74) gene underlie autosomal dominant woolly hair/hypotrichosis in Pakistani families

S. Basit, W. Ahmad, N. Ali, 2011, Human Genetics.

A novel insertion mutation in the cartilage-derived morphogenetic protein-1 (CDMP1) gene underlies Grebe-type chondrodysplasia in a consanguineous Pakistani family

S. Basit, W. Ahmad, G. Ali, 2008, BMC Medical Genetics.

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

S. Basit, W. Ahmad, G. Ali, 2009, Archives of Dermatological Research.

Two novel mutations in the gene EDAR causing autosomal recessive hypohidrotic ectodermal dysplasia.

W. Ahmad, N. Wasif, H. Javaid, 2011, Orthodontics & craniofacial research.

Genetic analysis of Xp22.3 micro-deletions in seventeen families segregating isolated form of X-linked ichthyosis.

S. Basit, W. Ahmad, Irfanullah, 2015, Journal of dermatological science.

A novel homozygous splice site variant in CERS3 causes autosomal recessive congenital ichthyosis

W. Ahmad, N. Wasif, Imran Ullah, 2023, Congenital Anomalies.

A new autosomal recessive nonsyndromic hearing impairment locus DFNB96 on chromosome 1p36.31-p36.13

S. Leal, S. Basit, W. Ahmad, 2011, Journal of Human Genetics.