Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Shouvik Sarker"'
Autor:
Hosneara Akter, Muhammad Mizanur Rahman, Shaoli Sarker, Mohammed Basiruzzaman, Md. Mazharul Islam, Md. Atikur Rahaman, Md. Ashiquir Rahaman, Tamannyat Binte Eshaque, Nushrat Jahan Dity, Shouvik Sarker, Md. Robed Amin, Mohammad Monir Hossain, Maksuda Lopa, Nargis Jahan, Shafaat Hossain, Amirul Islam, Ashaduzzaman Mondol, Md Omar Faruk, Narayan Saha, Gopen kumar Kundu, Shayla Imam Kanta, Rezaul Karim Kazal, Kanij Fatema, Md. Ashrafur Rahman, Maruf Hasan, Md. Abid Hossain Mollah, Md. Ismail Hosen, Noushad Karuvantevida, Ghausia Begum, Binte Zehra, Nasna Nassir, A. H. M. Nurun Nabi, K. M. Furkan Uddin, Mohammed Uddin
Publikováno v:
Frontiers in Genetics, Vol 14 (2023)
Introduction: Copy number variations (CNVs) play a critical role in the pathogenesis of neurodevelopmental disorders (NDD) among children. In this study, we aim to identify clinically relevant CNVs, genes and their phenotypic characteristics in an et
Externí odkaz:
https://doaj.org/article/990779ba5a7e42dc992125e6354c08cc
Publikováno v:
Dhaka University Journal of Biological Sciences. 29:209-218
This study was aimed at evaluating the association between gestational diabetes mellitus (GDM) and fetal birth weight considering duration of pregnancy, maternal age and body mass index (BMI). This was a retrospective cross-sectional study followed b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8a073a26ba44cb0efc576ae3511740e2
https://doi.org/10.3329/dujbs.v29i2.48764
https://doi.org/10.3329/dujbs.v29i2.48764
Autor:
Muhammad Mizanur Rahman, Hosneara Akter, Md. Ashiquir Rahaman, Md. Abid Hossain Mollah, Nushrat Jahan Dity, A.H.M. Nurun Nabi, Ashaduzzaman Mondol, Md. Robed Amin, Mohammed Basiruzzaman, Ghausia Begum, Maruf Hasan, Rezaul Karim Kazal, Narayan Saha, Gopenkumar Kundu, Md. Atikur Rahaman, Md. Ismail Hosen, Zehra Binte Ashraf, Amirul Islam, Maksuda Lopa, Shayla Imam Kanta, Mazharul M. Islam, Nargis Jahan, Mohammed Uddin, Shaoli Sarker, Md. Ashrafur Rahman, Shouvik Sarker, Omar Faruk, Tamannyat Binte Eshaque, Shafaat Hossain, K. M. Furkan Uddin, Noushad Karuvantevida, Monir Hossain, Nasna Nassir, Kanij Fatema
Background: Copy number variations (CNVs) play a critical role into the pathogenesis of neurodevelopmental disorders (NDD) among children. In this study, we aim to identify clinically relevant CNVs, genes and their phenotypic characteristics in an et
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fe1434565d248ccaf955acafc2020fd2
https://doi.org/10.21203/rs.3.rs-948388/v1
https://doi.org/10.21203/rs.3.rs-948388/v1
