1. Umair, Muhammad, Ahmed, Zaheer, Shaker, Bilal, Jawad Khan, Muhammad, Alfadhel, Majid. 2024. A novel homozygous FAM92A gene (CIBAR1) variant further confirms its association with non-syndromic postaxial polydactyly type A9 (PAPA9). In Clinical genetics, 106, 488-493. doi:10.1111/cge.14572. https://pubmed.ncbi.nlm.nih.gov/38853702/
2. Umair, Muhammad, Bilal, Muhammad, Ali, Raja H, Meitinger, Thomas, Ahmad, Wasim. 2019. Whole-exome sequencing revealed a nonsense mutation in STKLD1 causing non-syndromic pre-axial polydactyly type A affecting only upper limb. In Clinical genetics, 96, 134-139. doi:10.1111/cge.13547. https://pubmed.ncbi.nlm.nih.gov/30945277/
3. Bakar, Abu, Ullah, Asmat, Bibi, Nousheen, Ahmad, Wasim, Khan, Bushra. 2022. A novel homozygous variant in the GLI1 underlies postaxial polydactyly in a large consanguineous family with intra familial variable phenotypes. In European journal of medical genetics, 65, 104599. doi:10.1016/j.ejmg.2022.104599. https://pubmed.ncbi.nlm.nih.gov/36067927/
4. Umair, Muhammad, Ahmad, Farooq, Ahmad, Saeed, Ismail, Muhammad, Alfadhel, Majid. 2021. A Novel Homozygous Missense Mutation in the Zinc Finger DNA Binding Domain of GLI1 Causes Recessive Post-Axial Polydactyly. In Frontiers in genetics, 12, 746949. doi:10.3389/fgene.2021.746949. https://pubmed.ncbi.nlm.nih.gov/34721536/
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