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Clinical and genetic investigation of 14 families with various forms of short stature syndromes.
Khan FU, Khan H, Ullah K, Nawaz S, Abdullah, Khan MJ, Ahmed S, Ilyas M, Ali A, Ullah I, Sohail A, Hussain S, Ahmad F, Faisal, Sufyan R, Hayat A, Hanif T, Bibi F, Hayat M, Ullah R, Khan IU, Ali RH, Hasni MS, Ali H, Bilal M, Peralta S, Buchert R, Zehri Z, Hassan G, Liaqat K, Zahid M, Shah K, Mikitie O, Haack TB, Ji W, Lakhani SA, Ansar M, Ahmad W. Khan FU, et al. Among authors: ahmed s. Clin Genet. 2024 Sep;106(3):347-353. doi: 10.1111/cge.14550. Epub 2024 May 22. Clin Genet. 2024. PMID: 38774940
Variants in EFCAB7 underlie nonsyndromic postaxial polydactyly.
Bilal M, Khan H, Khan MJ, Haack TB, Buchert R, Liaqat K, Ullah K, Ahmed S, Bharadwaj T, Acharya A, Peralta S, Najumuddin, Ali H, Hasni MS, Schrauwen I, Ullah A, Ahmad W, Leal SM. Bilal M, et al. Among authors: ahmed s. Eur J Hum Genet. 2023 Nov;31(11):1270-1274. doi: 10.1038/s41431-023-01450-5. Epub 2023 Sep 8. Eur J Hum Genet. 2023. PMID: 37684519 Free PMC article.
Unraveling the Genetic Basis of Congenital Limb Anomalies in Eight Families.
Khan IU, Abdullah, Khan H, Ali A, Sani A, Khan FU, Ullah MT, Ahmed S, Liaqat R, Haider A, Ullah K, Ullah N, Khan MS, Hussain S, Ullah I, Ullah A, Anees M, Makitie O, Ahmad W. Khan IU, et al. Among authors: ahmed s. Clin Genet. 2024 Dec 5. doi: 10.1111/cge.14668. Online ahead of print. Clin Genet. 2024. PMID: 39639541
12,984 results
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