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Publikováno v:
Journal of Bangladesh College of Physicians & Surgeons. Jan2024, Vol. 42 Issue 1, p97-104. 8p.
Autor:
Wendt, Amanda S.1,2 (AUTHOR) amanda.wendt@pik-potsdam.de, Brintrup, Joaquin3 (AUTHOR), Waid, Jillian L.1,2,4 (AUTHOR), Kader, Abdul4 (AUTHOR), Lambrecht, Nathalie J.1,5 (AUTHOR), Gabrysch, Sabine1,2,5 (AUTHOR)
Publikováno v:
Orphanet Journal of Rare Diseases. 7/19/2023, Vol. 18 Issue 1, p1-11. 11p.
Autor:
Hasan, Md. Mahbub1 (AUTHOR) mahbub.hasan@cu.ac.bd, Uddin, Khaza Md. Kapil1 (AUTHOR), Lokman, Syed Mohammad1 (AUTHOR), Chakma, Kallyan1 (AUTHOR), Pulu, Aung Chaing-U1 (AUTHOR), Mannan, Adnan1 (AUTHOR), Raheem, Enayetur2 (AUTHOR), Chowdhury, Shahed Ahmad3,4 (AUTHOR), Hossain, Mohammad Sorowar2,5 (AUTHOR) mahbub.hasan@cu.ac.bd
Publikováno v:
PLoS ONE. 7/7/2023, Vol. 18 Issue 7, p1-13. 13p.
Autor:
Rakib, Nur Mohammad1 rakibcmc2006@gmail.com, Rishad, Mahbub Mayukh2, Prince, S. M. Kawser Zafor3, Jannat, Miftahul4, Khan, Tazbiha Rahman5, Zinan, Talha Islam6, Jeshan, Tanvir7, Kabir, Md. Alamgir8
Publikováno v:
Journal of Medicine. 2023, Vol. 24 Issue 2, p96-105. 10p.
Autor:
Selvaraj, Bhuvana1 sbhuvanarajesh@gmail.com, Subramanian, Ganesan2, Ramanathan, Senthil Kumar1, Soundararajan, Sangeetha3, Narayanasamy, Shettu3
Publikováno v:
AIMS Molecular Science. 2022, Vol. 9 Issue 3, p107-135. 29p.
Publikováno v:
Journal of Bangladesh College of Physicians & Surgeons. 2021, Vol. 39 Issue 3, p160-166. 7p.
Publikováno v:
Paediatric Nephrology Journal of Bangladesh; Jul-Dec2023, Vol. 8 Issue 2, p65-68, 4p
Prenatal Diagnosis and Screening of Thalassemia Mutations in Bangladesh: Presence of Rare Mutations.
Autor:
Aziz, Md. Abdul1 (AUTHOR), Khan, Waqar A.1 (AUTHOR), Banu, Bilquis2 (AUTHOR), Das, Sudipta A.1 (AUTHOR), Sadiya, Salma1 (AUTHOR), Begum, Sayeda3 (AUTHOR)
Publikováno v:
Hemoglobin. Nov2020, Vol. 44 Issue 6, p397-401. 5p.
Autor:
Noor, Farjana Akther1,2 (AUTHOR), Sultana, Nusrat1,3 (AUTHOR), Bhuyan, Golam Sarower1 (AUTHOR), Islam, Md Tarikul1 (AUTHOR), Hossain, Mohabbat1 (AUTHOR), Sarker, Suprovath Kumar1 (AUTHOR), Islam, Khaleda4 (AUTHOR), Khan, Waqar Ahmed5 (AUTHOR), Rahman, Mujahida6 (AUTHOR), Qadri, Syeda Kashfi7 (AUTHOR), Shekhar, Hossain Uddin2 (AUTHOR), Qadri, Firdausi1,8 (AUTHOR), Qadri, Syed Saleheen1 (AUTHOR), Mannoor, Kaiissar1 (AUTHOR) kaiissar@ideshi.org
Publikováno v:
Orphanet Journal of Rare Diseases. 1/15/2020, Vol. 15 Issue 1, p1-12. 12p.