Hammal U. Khan
Islamabad, IS, Pakistan
Last Updated: 09/26/2026
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Found 26 publications
HOXD12 a candidate gene for a novel form of synpolydactyly.
Journal: Bone
Published: December 10, 2025
A novel loss-of-function variant in DNHD1 linked to human asthenozoospermia.
Journal: Clinical and experimental reproductive medicine
Published: November 27, 2025
Further Evidence for LRRC7 Gene Involvement in Neurodevelopmental Disorder: A Novel Variant.
Journal: The journal of gene medicine
Published: September 24, 2025
Structural dynamics and stability analysis of a novel ARSK variant confirms its role in MPS type X pathogenesis.
Journal: Glycoconjugate journal
Published: September 08, 2025
Novel KIAA0825 Variants Underlie Nonsyndromic Postaxial Polydactyly.
Journal: Genes
Published: July 24, 2025
Bi-Allelic DSG1 Splice-Site Variant Identified in a Family With Non-Syndromic Striate Palmoplantar Keratoderma.
Journal: The Journal of dermatology
Published: June 30, 2025
Unraveling the Genetic Basis of Congenital Limb Anomalies in Eight Families.
Journal: Clinical genetics
Published: September 12, 2024
Novel pathogenic variants in HR underlie atrichia with papular lesions in a cohort of 10 families.
Journal: The Journal of dermatology
Published: May 15, 2024
A novel homozygous FAM92A gene (CIBAR1) variant further confirms its association with non-syndromic postaxial polydactyly type A9 (PAPA9).
Journal: Clinical genetics
Published: March 25, 2024
Clinical and genetic investigation of 14 families with various forms of short stature syndromes.
Journal: Clinical genetics
Published: March 14, 2024
A Novel Variant in the Cyto-Tail of SMO Gene Underlying Isolated Postaxial Polydactyly.
Journal: Molecular syndromology
Published: March 04, 2024
Last Updated: 09/26/2026