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.
8. A Novel Mutation of the α2-Globin Gene Causing α Chen B; Lin L; Yi S; Chen Q; Wei H; Li G; Zheng C; He S; Qiu X Hemoglobin; 2017 Jan; 41(1):56-58. PubMed ID: 28395547 [TBL] [Abstract][Full Text] [Related]
9. Hb Adana (HBA2 or HBA1: c.179G > A) and alpha thalassemia: Genotype-phenotype correlation. Singh SA; Sarangi S; Appiah-Kubi A; Hsu P; Smith WB; Gallagher PG; Glader B; Chui DHK Pediatr Blood Cancer; 2018 Sep; 65(9):e27220. PubMed ID: 29749692 [TBL] [Abstract][Full Text] [Related]
10. Hemoglobin profile and molecular characteristics of the complex interaction of hemoglobin Doi-Saket [α9(A7) asn > lys, HBA2:c.30C > a], a novel α2α1 hybrid globin variant, with hemoglobin E [β26(B8) Glu > lys, HBB:c.79G > A] and deletional α Panyasai S; Khongthai K; Satthakarn S Ann Med; 2023; 55(2):2264174. PubMed ID: 37796611 [TBL] [Abstract][Full Text] [Related]
12. Novel α-Globin Splice Site Mutation (HBA2: c.96-5C>A) in Combination with Three-Gene Deletion Hb H Disease. Van de Water N; Tan T; Crowley M; Kerr R; Browett P Hemoglobin; 2018 Mar; 42(2):122-125. PubMed ID: 30200833 [TBL] [Abstract][Full Text] [Related]
13. Complex interaction of hemoglobin (Hb) Nakhon Ratchasima [α63(E12)Ala→Val], a novel α2-globin chain variant with Hb E [β26(B8)Glu→Lys] and a deletional α(+)-thalassemia. Srivorakun H; Fucharoen G; Puangplruk R; Kheawon N; Fucharoen S Eur J Haematol; 2011 Jul; 87(1):68-72. PubMed ID: 21447006 [TBL] [Abstract][Full Text] [Related]
14. Hb Iberia [α104(G11)Cys → Arg,TGC>CGC (α2) (HBA2:c.313T>C)], a new α-thalassemic hemoglobin variant found in the Iberian Peninsula: report of six cases. Bento C; Oliveira AC; Neves J; Gameiro M; Cunha E; Coucelo M; Costa RM; Barbot J; Costa E; Fernández-Lago C; Ribeiro ML Hemoglobin; 2012; 36(6):517-25. PubMed ID: 23181747 [TBL] [Abstract][Full Text] [Related]
15. In vitro characterization of the α-thalassemia point mutation HBA2:c.95+1G>A [IVS-I-1(G>A) (α2)]. Qadah T; Finlayson J; Ghassemifar R Hemoglobin; 2012; 36(1):38-46. PubMed ID: 21967524 [TBL] [Abstract][Full Text] [Related]
16. Association of Hb Shenyang [α26(B7)Ala→Glu, G Panyasai S; Kongthai K; Phasit A Hemoglobin; 2020 Sep; 44(5):354-360. PubMed ID: 33023349 [TBL] [Abstract][Full Text] [Related]
17. A case series of α-thalassemia intermedia due to compound heterozygosity for Hb Adana [HBA2: c179G>A (or HBA1); p.Gly60Asp] with other α-thalassemias in Malay families. Alauddin H; Jaapar NA; Azma RZ; Ithnin A; Razak NF; Loh CK; Alias H; Abdul-Latiff Z; Othman A Hemoglobin; 2014; 38(4):277-81. PubMed ID: 24829075 [TBL] [Abstract][Full Text] [Related]
18. A Wide Spectrum Study of α-Globin Chain Variants: Cases from the UK. Khalil MSM; Timbs AT; Henderson SJ; Schuh A; El-Khawanky MM; Old JM Hemoglobin; 2020 May; 44(3):195-200. PubMed ID: 32597250 [TBL] [Abstract][Full Text] [Related]
19. α-Thalassemia Intermedia Results from Interactions of Unstable Hb Prato [α31(B12)Arg→Ser ( Panyasai S; Phasit A Hemoglobin; 2020 Jul; 44(4):264-271. PubMed ID: 32727229 [TBL] [Abstract][Full Text] [Related]
20. Two new hemoglobin variants: Hb Aix-Les-Bains [β5(A2)Pro→Leu; HBB:c.17 C>T] and Hb Dubai [α122(H5)His→Leu (α2); HBA2:c.368 A>T]. Joly P; Garcia C; Lacan P; Couprie N; Francina A Hemoglobin; 2011; 35(2):147-51. PubMed ID: 21417572 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]