Khadim Shah
5PUBLICATIONS
6CO-AUTHORS
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Publications (5)
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|May 22, 2024
Clinical and genetic investigation of 14 families with various forms of short stature syndromes.Fati Ullah Khan, Hammal Khan, Kifayat Ullah
|Jun 13, 2023
Nonsense variant in a consanguineous family expands the phenotype of KPTN gene-related syndrome to include hearing impairment.Khurram Liaqat, Thashi Bharadwaj, Khadim Shah
|Feb 15, 2023
Biallelic mutations in FLG, TGM1, and STS genes segregated with different types of ichthyoses in eight families of Pakistani origin.Niamatullah Khan, Khadim Shah, Fozia Fozia
|May 12, 2019
Biallelic mutations in the LPAR6 gene causing autosomal recessive wooly hair/hypotrichosis phenotype in five Pakistani families.Ghulam M Khan, Noor Hassan, Niamatullah Khan
|Nov 14, 2017
Sequence variants in nine different genes underlying rare skin disorders in 10 consanguineous families.Khadim Shah, Sabba Mehmood, Abid Jan
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