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4. Hb Cardarelli [beta86(F2)Ala-->Pro]: a new unstable and hyperaffine variant in association with beta(+)-thalassemia. Pagano L; Salzano AM; Carbone V; Iannelli D; Viola A; Pollio F; Prossomariti L; David O; Ricco G; Pucci P Hemoglobin; 2004 May; 28(2):103-15. PubMed ID: 15182052 [TBL] [Abstract][Full Text] [Related]
5. Hb Marineo [beta70(E14)Ala-->Val]: a silent hemoglobin variant with a mutation within the heme pocket. Giambona A; Vinciguerra M; Cassarà F; Li Muli R; Leto F; Passarello C; Wajcman H; Maggio A Hemoglobin; 2006; 30(2):139-48. PubMed ID: 16798637 [TBL] [Abstract][Full Text] [Related]
6. Mutational spectrum of delta-globin gene in the Portuguese population. Morgado A; Picanço I; Gomes S; Miranda A; Coucelo M; Seuanes F; Seixas MT; Romão L; Faustino P Eur J Haematol; 2007 Nov; 79(5):422-8. PubMed ID: 17916081 [TBL] [Abstract][Full Text] [Related]
7. Four new beta chain hemoglobin variants without clinical or hematological effects: Hb San Bruno [beta39(C5)Gln-->His]; Hb Fort Dodge [beta93(F9)Cys-Tyr]; Hb Rhode Island [beta116(G18)His-->Tyr]; and Hb Inglewood [beta142(H20)Ala-->Thr]. Hoyer JD; McCormick DJ; Snow K; Kubik KS; Holmes MW; Dawson DB; Shaber R; Marner M; Hosmer J; Shinno N; Fairbanks VF Hemoglobin; 2002 Aug; 26(3):299-303. PubMed ID: 12403495 [No Abstract] [Full Text] [Related]
8. Two new hemoglobin variants with increased oxygen affinity: Hb Nantes [beta34(B16)Val-->Leu] and Hb Vexin [beta116(G18)His-->Leu]. Wajcman H; Bardakdjian-Michau J; Riou J; Préhu C; Kister J; Baudin-Creuza V; Promé D; Richelme-David S; Harousseau JL; Galactéros F Hemoglobin; 2003 Aug; 27(3):191-9. PubMed ID: 12908805 [No Abstract] [Full Text] [Related]
9. A new δ chain variant, Hb A2-Tunis [δ46(CD5)Gly → Glu; HBD: c.140G>A], observed in a Tunisian family in association with a compound heterozygosity for Hb C [β6(A3)Glu → Lys; HBB: c.19G>A] β(0)-thalassemia [IVS-I-1 (β143, G>A); HBB: c.92+1G>A]. Moumni I; Zorai A; Mahjoub S; Mosbahi I; Chaouechi D; Benromdhane N; Abbes S Hemoglobin; 2014; 38(2):88-90. PubMed ID: 24471655 [TBL] [Abstract][Full Text] [Related]
10. Heterozygosity for the IVS-I-5 (G-->C) mutation with a G-->A change at codon 18 (Val-->Met; Hb Baden) in cis and a T-->G mutation at codon 126 (Val-->Gly; Hb Dhonburi) in trans resulting in a thalassemia intermedia. Divoky V; Bissé E; Wilson JB; Gu LH; Wieland H; Heinrichs I; Prior JF; Huisman TH Biochim Biophys Acta; 1992 Dec; 1180(2):173-9. PubMed ID: 1463768 [TBL] [Abstract][Full Text] [Related]
11. A Clinical Update of the Hb Siirt [β27(B9)Ala→Gly; HBB: c.83C>G] Hemoglobin Variant. Cappabianca MP; Colosimo A; Sabatucci A; Dainese E; Di Biagio P; Piscitelli R; Sarra O; Zei D; Amato A Hemoglobin; 2017 Jan; 41(1):53-55. PubMed ID: 28391745 [TBL] [Abstract][Full Text] [Related]
12. Two new delta-globin mutations: Hb A2-Ninive [delta133(H11)Val-Ala] and a delta(+)-thalassemia mutation [-31 (A --> G)] in the TATA box of the delta-globin gene. Frischknecht H; Dutly F Hemoglobin; 2005; 29(2):151-4. PubMed ID: 15921167 [TBL] [Abstract][Full Text] [Related]
13. Erythrocytosis due to a combination of the high oxygen affinity hemoglobin variant, Hb Olympia [beta20(B2)Val-->Met] with beta- and alpha-thalassemia mutations: first case in the literature. Kalotychou V; Tzanetea R; Konstantopoulos K; Papassotiriou I; Rombos I Hemoglobin; 2010; 34(4):383-8. PubMed ID: 20642336 [TBL] [Abstract][Full Text] [Related]
14. Hb Leeds [beta56(D7)Gly-->Cys]: a new hemoglobin that aggravates anemia in a child with beta(0)-thalassemia trait. Williams JP; Scrivens JH; Green BN; Farrar LM; Sutcliffe M Hemoglobin; 2007; 31(3):367-73. PubMed ID: 17654074 [TBL] [Abstract][Full Text] [Related]
15. A new G(gamma) chain variant: Hb F-Bron [gamma20(B2)val-->Ala]. Lacan P; Burnichon N; Becchi M; Zanella-Cleon I; Aubry M; Couprie N; Francina A Hemoglobin; 2005; 29(4):301-5. PubMed ID: 16370494 [TBL] [Abstract][Full Text] [Related]
17. Hb Bronte or alpha93(FG5)Val-->Gly: a new unstable variant of the alpha2-globin gene, associated with a mild alpha(+)-thalassemia phenotype. Lacerra G; Testa R; De Angioletti M; Schilirò G; Carestia C Hemoglobin; 2003 Aug; 27(3):149-59. PubMed ID: 12908799 [TBL] [Abstract][Full Text] [Related]
18. Co-inheritance of Hb Hershey [beta70(E14) Ala-->Gly] and Hb La Pommeraie [beta133(H11)Val-->Met] in a Sicilian subject. Giambona A; Vinciguerra M; Passarello C; La Rosa MA; Lo Giudice G; Di Bella C; Amorini M; Iacona F; Salpietro C; Maggio A; Rigoli L Eur J Haematol; 2010 May; 84(5):453-7. PubMed ID: 20059533 [TBL] [Abstract][Full Text] [Related]
19. Compound heterozygosity for unstable hemoglobin Genova and beta(o)-thalassemia associated with early onset of thalassemia major syndrome. Badens C; Paolasso C; Fossat C; Wajcman H; Thuret I Haematologica; 2005 Jan; 90(1):ECR04. PubMed ID: 15653458 [TBL] [Abstract][Full Text] [Related]
20. Hb Sun Prairie: diagnostic pitfalls in thalassemic hemoglobinopathies. Ho PJ; Rochette J; Rees DC; Fisher CA; Huehns ER; Will AM; Thein SL Hemoglobin; 1996 May; 20(2):103-12. PubMed ID: 8811313 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]