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Hemoglobin|July 9, 2015
Sudanese (δβ)0-Thalassemia: Identification and Characterization of a Novel 9.6 kb DeletionJohn S Waye, Barry Eng, Tiffany Got, 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|June 27, 2006
Three new alpha-thalassemia point mutations ascertained through newborn screeningBarry Eng, Margie Patterson, Lynda Walker, et al.Annals of the New York Academy of Sciences|December 13, 2005
Prenatal diagnosis of hemoglobinopathies in Ontario, CanadaRaveen K Basran, Margie Patterson, Lynda Walker, et al.Hemoglobin|June 10, 2026
Hb F-SickKids (HBG2: C.308A > G): A Novel γ-Globin Variant Associated with Transient Neonatal CyanosisLandry E Nfonsam, Meredith Hanna, Lisa Nakamura, et al.American Journal of Hematology|October 31, 2003
Beta-thalassemia in association with a new delta-chain hemoglobin variant [delta116(g18)Arg-->Leu]: implications for carrier screening and prenatal diagnosisJohn S Waye, Margaret Patterson, Lynda Walker, et al.Pageof 3