Hammal Khan

4PUBLICATIONS
7CO-AUTHORS
Neurology and neuromuscular diseasesNeurogeneticsAnthropological geneticsPacific Peoples youth and family
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Publications (4)

|May 19, 2026
Homozygous Variant in NADSYN1 Causes Multiple Congenital Vertebral Malformation, With Neurodevelopmental Disorder.

|Mar 31, 2026
Further Evidence for LRRC7 Gene Involvement in Neurodevelopmental Disorder: A Novel Variant.

Shazia Khan, Muhammad Bilal, Hammal Khan

|Sep 27, 2025
Novel KIAA0825 Variants Underlie Nonsyndromic Postaxial Polydactyly.

Abdullah, Thashi Bharadwaj, Saffia Javed

|Aug 11, 2023
A variant in the LDL receptor-related protein encoding gene LRP4 underlying polydactyly and phalangeal synostosis in a family of Pakistani origin.

Hammal Khan, Kifayat Ullah, Abid Jan

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Frequent Collaborators

1 joint publications

Kifayat Ullah

1 joint publications

Wasim Ahmad

1 joint publications

Thashi Bharadwaj

1 joint publications

Saffia Javed