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Hemoglobin|July 9, 2024
Point-of-Care Newborn Screening for Sickle Cell Disease at Selected Health Facilities in the GambiaSamuel Ademola Adegoke, Lamin Makalo, Adama Sallah, et al.Hemoglobin|January 8, 2024
Strengthening Health System and Community Mobilization for Sickle Cell Disease Screening and Management among Tribal Populations in India: An Interventional StudyBontha V Babu, Yogita Sharma, Parikipandla Sridevi, et al.Hemoglobin|December 26, 2023
The Spectrum of α-Thalassemia Mutations in Syrian PatientsHossam Murad, Faten Moassas, Bouthina Ali, et al.Hemoglobin|January 19, 2024
Misdiagnosis of β-Thalassemia Major Due to Chinese Gγ+(Aγδβ)0-Thalassemia Combined with β0-ThalassemiaLi-Hong Zheng, Liang Liang, Jin-Ping Bai, et al.Hemoglobin|March 1, 2024
β0-Thalassemia Caused by a Novel Nonsense Mutation [HBB:c.199A > T]John S Waye, Meredith Hanna, Betty-Ann Hohenadel, et al.Hemoglobin|February 15, 2024
Splice Acceptor Mutation [HBB:c.93-2A > T] in a Patient with Hb S/β0-ThalassemiaJohn S Waye, Meredith Hanna, Lisa Nakamura, et al.Hemoglobin|April 2, 2024
Thrombosis Tendency After Splenectomy in a Danish Family With Hemoglobin Volga, and a Literature ReviewJohanne Kodal Breinholt, Andreas Glenthøj, Mustafa Vakur BorHemoglobin|April 23, 2024
A Novel Frameshift Mutation(HBA2:C.337delC) Associated With α-Thalassemia Trait Detected by Next-Generation Sequencing in Southern ChinaLei Pan, Yan Wang, Haiying Lin, et al.Hemoglobin|September 28, 2023
Development of a Quantitative Multiplex PCR to Detect Three Common Alpha Thalassemia DeletionsZahra Hajimohammadi, Sara Alimohammadi-Bidhendi, Fahimeh Bagheri Amiri, et al.Hemoglobin|September 23, 2024
Characterization of Hemoglobin Malay Phenotypes in Tertiary HospitalsAlia Suzana Asri, Muhammad Hafiz Samsuddin, Norunaluwar Jalil, et al.Pageof 238