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Hemoglobin|August 26, 2017
α0-Thalassemia Due to a 90.7 kb Deletion (- -NFLD)John S Waye, Barry Eng, Meredith Hanna, 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|May 9, 2013
Mild β(+)-thalassemia associated with two linked sequence variants: IVS-II-839 (T>C) and IVS-II-844 (C>A)John S Waye, Barry Eng, Laurie Hellens, et al.
Hemoglobin|August 7, 2009
Three new beta-thalassemia mutations with varying degrees of severityHannes Frischknecht, Fabrizio Dutly, Lynda Walker, et al.
Hemoglobin|February 13, 2013
Normal Hb A2 β-thalassemia trait: frameshift mutation (HBB: c.187_251dup) in cis with the Hb A2' δ-globin gene missense mutation (HBD: c.49G>C)John S Waye, Barry Eng, Laurie Hellens, et al.
Hemoglobin|April 22, 2015
α(+)-Thalassemia Due to a Frameshift Mutation of the α2-Globin Gene [codons 55/56 (+T) or HBA2: c.168dup]John S Waye, Barry Eng, Meredith Hanna, et al.
Hemoglobin|November 19, 2014
Non-thalassemic phenotype associated with the -83 (G > A) mutation of the β-globin gene promoter (HBB: c.-133G > A)John S Waye, Barry Eng, Meredith Hanna, et al.
Hemoglobin|May 9, 2007
Three new beta-globin gene promoter mutations identified through newborn screeningBarry Eng, Lynda Walker, Lisa M Nakamura, et al.
Hemoglobin|July 21, 2010
Characterization of three novel delta chain hemoglobin variants and two delta-thalassemia allelesHannes Frischknecht, Heinz Troxler, Fabrizio Dutly, et al.
Hemoglobin|April 2, 2024
Newborn Screening for β-Thalassemia Identifies a Complex Genotype Involving a Novel β-Globin Gene Mutation (HBB:c.336dup)John S Waye, Meredith Hanna, Betty-Ann Hohenadel, et al.
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