These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
12. Distinct phenotypic expression associated with a new hyperunstable alpha globin variant (Hb heraklion, alpha1cd37(C2)Pro>0): comparison to other alpha-thalassemic hemoglobinopathies. Traeger-Synodinos J; Papassotiriou I; Metaxotou-Mavrommati A; Vrettou C; Stamoulakatou A; Kanavakis E Blood Cells Mol Dis; 2000 Aug; 26(4):276-84. PubMed ID: 11042028 [TBL] [Abstract][Full Text] [Related]
13. Elevated Hb A₂ Levels in a Patient with a Compound Heterozygosity for the (β⁺) -31 (A > G) and (β⁰) Codon 17 (A > T) Mutations Together with a Single α-Globin Gene. Panyasai S; Jaiping K; Pornprasert S Hemoglobin; 2015; 39(4):292-5. PubMed ID: 26029792 [TBL] [Abstract][Full Text] [Related]
14. First Report of a Dominantly Inherited β-Thalassemia Caused by a Novel Elongated β-Globin Chain. Farashi S; Rad F; Shahmohammadi B; Imanian H; Azarkeivan A; Najmabadi H Hemoglobin; 2016; 40(2):102-7. PubMed ID: 26850598 [TBL] [Abstract][Full Text] [Related]
15. Molecular Characterization and Hematological Aspects of Hb E-Myanmar [β26(B8)Glu→Lys and β65(E9)Lys→Asn, Satthakarn S; Boonmee S; Panyasai S Hemoglobin; 2020 Nov; 44(6):385-390. PubMed ID: 33222574 [TBL] [Abstract][Full Text] [Related]
16. Molecular and phenotype characterization of an elongated β-globin variant produced by HBB:C.313delA. Lin W; Zhang Q; Shen Z; Qu X; Wang Q; Wei L; Qiu Y; Yang J; Xu X; Lao J Int J Lab Hematol; 2021 Dec; 43(6):1620-1627. PubMed ID: 34271589 [TBL] [Abstract][Full Text] [Related]
17. New and known β-thalassemia determinants masked by known and new δ gene defects [Hb A(2)-Ramallah or δ6(A3)Glu→Gln, GAG>>CAG]. Phylipsen M; Harteveld CL; de Metz M; Gallivan MV; Arkesteijn SG; Luo HY; Chui DH; Giordano PC Hemoglobin; 2010; 34(5):445-50. PubMed ID: 20854118 [TBL] [Abstract][Full Text] [Related]
18. Hb Ryazan: An Elongated C-Terminal β-Chain Due to a New Frameshift Mutation, HBB: c.396delG p.Val133Trpfs*25. Demidova E; Salomashkina V; Selivanova D; Litvin E; Karamyan N; Mann S; Dvirnyk V; Maryina S; Petrova N; Gorgidze L; Peredel'skaya A; Tsvetaeva N; Smetanina N; Surin V Hemoglobin; 2023 Nov; 47(2):97-101. PubMed ID: 37194736 [TBL] [Abstract][Full Text] [Related]