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Expanding deep phenotypic spectrum associated with atypical pathogenic structural variations overlapping 15q11-q13 imprinting region.
Brain Behav. 2024 Apr;14(4):e3437. doi: 10.1002/brb3.3437.
Brain Behav. 2024.
PMID: 38616334
Free PMC article.
Mutational spectrum and phenotypic variability of Duchenne muscular dystrophy and related disorders in a Bangladeshi population.
Sarker S, Eshaque TB, Soorajkumar A, Nassir N, Zehra B, Kanta SI, Rahaman MA, Islam A, Akter S, Ali MK, Mim RA, Uddin KMF, Chowdhury MSJ, Shams N, Baqui MA, Lim ET, Akter H, Woodbury-Smith M, Uddin M.
Sarker S, et al. Among authors: eshaque tb.
Sci Rep. 2023 Dec 6;13(1):21547. doi: 10.1038/s41598-023-48982-w.
Sci Rep. 2023.
PMID: 38057384
Free PMC article.
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Construction of copy number variation landscape and characterization of associated genes in a Bangladeshi cohort of neurodevelopmental disorders.
Akter H, Rahman MM, Sarker S, Basiruzzaman M, Islam MM, Rahaman MA, Rahaman MA, Eshaque TB, Dity NJ, Sarker S, Amin MR, Hossain MM, Lopa M, Jahan N, Hossain S, Islam A, Mondol A, Faruk MO, Saha N, Kundu GK, Kanta SI, Kazal RK, Fatema K, Rahman MA, Hasan M, Hossain Mollah MA, Hosen MI, Karuvantevida N, Begum G, Zehra B, Nassir N, Nabi AHMN, Uddin KMF, Uddin M.
Akter H, et al. Among authors: eshaque tb.
Front Genet. 2023 Mar 7;14:955631. doi: 10.3389/fgene.2023.955631. eCollection 2023.
Front Genet. 2023.
PMID: 36959829
Free PMC article.
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