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Molecular Syndromology|March 29, 2021
A Frameshift Variant in KIAA0825 Causes Postaxial PolydactylyMuhammad Bilal, Wasim Ahmad
Frontiers in Genetics|November 22, 2018
Clinical Genetics of Polydactyly: An Updated ReviewMuhammad Umair, Farooq Ahmad, Muhammad Bilal, et al.
Molecular Biology Reports|October 28, 2023
Sequence variants in different genes underlying Bardet-Biedl syndrome in four consanguineous familiesAmjad Ali, Abdullah, Muhammad Bilal, et al.
Annals of Human Genetics|January 12, 2018
A novel homozygous variant in BMPR1B underlies acromesomelic dysplasia Hunter-Thompson typeAsmat Ullah, Muhammad Umair, Dost Muhammad, et al.
Bone|March 5, 2026
HOXD12 a candidate gene for a novel form of synpolydactylyHammal Khan, Muhammad Bilal, Thashi Bharadwaj, et al.
Molecular Syndromology|December 7, 2023
Sequence Variants in the WNT10B Underlying Non-Syndromic Split-Hand/Foot MalformationMuhammad Bilal, Tobias B Haack, Rebecca Buchert, et al.
Molecular Syndromology|June 16, 2023
Sequence Variants in MEGF8 and GJA1 Underlying SyndactylyMuhammad Bilal, Tobias B Haack, Rebecca Buchert, et al.
Genetic Testing and Molecular Biomarkers|October 2, 2019
Variants in GLI3 Cause Greig Cephalopolysyndactyly SyndromeAbdullah, Maryam Yousaf, Zahid Azeem, et al.
The Journal of Gene Medicine|August 28, 2023
A variant in sperm-specific glycolytic enzyme enolase 4 (ENO4) causes human male infertilityShoaib Nawaz, Shabir Hussain, Muhammad Bilal, et al.
European Journal of Medical Genetics|August 15, 2018
A novel insertion and deletion mutation in the BHLHA9 underlies polydactyly and mesoaxial synostotic syndactyly with phalangeal reductionAsmat Ullah, Raja Hussain Ali, Ayesha Isani Majeed, et al.
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