Genomic insights from a deeply phenotyped highly consanguineous neurodevelopmental disorders cohort.
Akter H, Rahaman MA, Eshaque TB, Mohamed N, Islam A, Morshed M, Shahin Z, Muhaimin A, Foyzullah AM, Mim RA, Omar FB, Hasan MN, Satsangi D, Ahmed N, Al Saba A, Jahan N, Hossen MA, Mondol MA, Sakib AS, Kabir R, Jahan Chowdhury MS, Shams N, Afroz S, Kanta SI, Bhuiyan SJ, Biswas R, Hanif S, Tambi R, Nassir N, Rahman MM, Duan J, D Børglum A, Amin R, Basiruzzaman M, Kamruzzaman M, Sarker S, Woodbury-Smith M, Uddin KMF, Nabi AHMN, Uddin M.
Akter H, et al. Among authors: hossen ma.
Genet Med. 2024 Sep 26;27(1):101282. doi: 10.1016/j.gim.2024.101282. Online ahead of print.
Genet Med. 2024.
PMID: 39342494
Free article.