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pro vyhledávání: '"KM Furkan Uddin"'
Autor:
Muhammad M. Rahman, KM Furkan Uddin, Nesreen K. Al Jezawi, Noushad Karuvantevida, Hosneara Akter, Nushrat J. Dity, Md. Ashiquir Rahaman, Maksuda Begum, Md. Atikur Rahaman, Md. Abdul Baqui, Zeena Salwa, Serajul Islam, Marc Woodbury‐Smith, Mohammed Basiruzzaman, Mohammed Uddin
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 7, Iss 10, Pp n/a-n/a (2019)
Abstract Background Intellectual disability (ID) is a complex condition that can impact multiple domains of development. The genetic contribution to ID’s etiology is significant, with more than 100 implicated genes and loci currently identified. Th
Externí odkaz:
https://doaj.org/article/6991731ee49c418aabb747b9a403609a
Autor:
Akter H; Genetics and Genomic Medicine Centre, NeuroGen Children's Healthcare, Dhaka, Bangladesh.; Department of Biochemistry and Molecular Biology, University of Dhaka, Dhaka, Bangladesh., Hossain MS; Department of Genetic Engineering & Biotechnology, University of Dhaka, Dhaka, Bangladesh., Dity NJ; Genetics and Genomic Medicine Centre, NeuroGen Children's Healthcare, Dhaka, Bangladesh., Rahaman MA; Genetics and Genomic Medicine Centre, NeuroGen Children's Healthcare, Dhaka, Bangladesh., Furkan Uddin KM; Genetics and Genomic Medicine Centre, NeuroGen Children's Healthcare, Dhaka, Bangladesh., Nassir N; College of Medicine, Mohammed Bin Rashid University of Medicine and Health Science, Dubai, UAE., Begum G; College of Medicine, Mohammed Bin Rashid University of Medicine and Health Science, Dubai, UAE., Hameid RA; College of Medicine, Mohammed Bin Rashid University of Medicine and Health Science, Dubai, UAE., Islam MS; BioTED, Dhaka, Bangladesh., Tusty TA; Department of Genetic Engineering & Biotechnology, University of Dhaka, Dhaka, Bangladesh., Basiruzzaman M; Genetics and Genomic Medicine Centre, NeuroGen Children's Healthcare, Dhaka, Bangladesh.; Department of Child Neurology, NeuroGen Children's Healthcare, Dhaka, Bangladesh., Sarkar S; Genetics and Genomic Medicine Centre, NeuroGen Children's Healthcare, Dhaka, Bangladesh.; Department of Child Neurology, NeuroGen Children's Healthcare, Dhaka, Bangladesh., Islam M; Genetics and Genomic Medicine Centre, NeuroGen Children's Healthcare, Dhaka, Bangladesh.; Department of Child Neurology, NeuroGen Children's Healthcare, Dhaka, Bangladesh., Jahan S; Department of Endocrinology & Metabolism, Bangabandhu Sheikh Mujib Medical University, Dhaka, Bangladesh., Lim ET; Department of Genetics, Harvard Medical School, Boston, USA., Woodbury-Smith M; The Centre for Applied Genomics, The Hospital for Sick Children, Toronto, Canada.; Translational and Clinical Research Institute, Newcastle University, Newcastle upon Tyne, UK., Stavropoulos DJ; Genome Diagnostics, Department of Pediatric Laboratory Medicine, The Hospital for Sick Children, Toronto, Canada., O'Rielly DD; Faculty of Medicine, Memorial University, St. John's, NL, Canada., Berdeiv BK; College of Medicine, Mohammed Bin Rashid University of Medicine and Health Science, Dubai, UAE., Nurun Nabi AHM; Department of Biochemistry and Molecular Biology, University of Dhaka, Dhaka, Bangladesh., Ahsan MN; Department of Genetic Engineering & Biotechnology, University of Dhaka, Dhaka, Bangladesh., Scherer SW; The Centre for Applied Genomics, The Hospital for Sick Children, Toronto, Canada.; McLaughlin Centre and Department of Molecular Genetics, University of Toronto, Toronto, Ontario, Canada., Uddin M; College of Medicine, Mohammed Bin Rashid University of Medicine and Health Science, Dubai, UAE. mohammed.uddin@mbru.ac.ae.
Publikováno v:
NPJ genomic medicine [NPJ Genom Med] 2021 Feb 16; Vol. 6 (1), pp. 14. Date of Electronic Publication: 2021 Feb 16.