Sulman Basit
www.mendeley.com
0000-0003-4294-6825
Taibah University
3 papers found
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The Expansion of the Spectrum in Stuttering Disorders to a Novel ARMC Gene Family (ARMC3)
Novel Homozygous Mutations in the Genes TGM1, SULT2B1, SPINK5 and FLG in Four Families Underlying Congenital Ichthyosis
Biallelic mutations in the LPAR6 gene causing autosomal recessive wooly hair/hypotrichosis phenotype in five Pakistani families
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