106 related articles for article (PubMed ID: 12972031)
1. Short insertion in a hemoglobin chain: Hb Esch, an unstable alpha1 variant with duplication of the sequence Ala65-Leu-Thr-Asn68.
Préhu C; Groff P; Kalmes G; Golinska B; Riou J; Prome D; Richelme-David S; Kiger L; Ducrocq R; Wajcman H
Blood Cells Mol Dis; 2003; 31(2):234-9. PubMed ID: 12972031
[TBL] [Abstract][Full Text] [Related]
2. Novel hemoglobin alpha chain elongation resulting from a 15-residue insertion and tandem duplication of the F helix.
Brennan SO; Owen MC; Chan T; Ruskova A
Clin Biochem; 2008 Oct; 41(14-15):1156-61. PubMed ID: 18571503
[TBL] [Abstract][Full Text] [Related]
3. Hb Bleuland [alpha108(G15)Thr-->Asn, ACC-->AAC (alpha2)]: a new abnormal hemoglobin associated with a mild alpha-thalassemia phenotype.
Harteveld CL; Versteegh FG; Kok PJ; van Rooijen-Nijdam IH; van Delft P; Giordano PC
Hemoglobin; 2006; 30(3):349-54. PubMed ID: 16840225
[TBL] [Abstract][Full Text] [Related]
4. Description of two new alpha variants: Hb Canuts [alpha85(F6)Asp-->His (alpha1)] and Hb Ambroise Pare [alpha117(GH5)Phe-->Ile (alpha2)]; two new beta variants: Hb Beaujolais [beta84(EF8)Thr-->Asn] and Hb Monplaisir [beta147 (Tyr-Lys-Leu-Ala-Phe-Phe-Leu-Leu-Ser-Asn-Phe-Tyr-158-COOH)] and one new delta variant: Hb (A2)North Africa [delta59(E3)Lys-->Met].
Joly P; Lacan P; Bererd M; Garcia C; Zanella-Cleon I; Becchi M; Aubry M; Couprie N; Francina A
Hemoglobin; 2009; 33(3):196-205. PubMed ID: 19657833
[TBL] [Abstract][Full Text] [Related]
5. Hb Evora [alpha2-35 (B16), Ser-->Pro], a novel hemoglobin variant associated with an alpha-thalassemia phenotype.
Gomes S; Picanço I; Miranda A; Seixas MT; Oliveira M; Romão L; Faustino P
Haematologica; 2007 Feb; 92(2):252-3. PubMed ID: 17296578
[TBL] [Abstract][Full Text] [Related]
6. Unstable alpha-chain hemoglobin variants with factitious beta-thalassemia biosynthetic ratio: Hb Questembert (alpha 131[H14]Ser-->Pro) and Hb Caen (alpha 132[H15]Val-->Gly).
Wajcman H; Vasseur C; Blouquit Y; Rosa J; Labie D; Najman A; Reman O; Leporrier M; Galacteros F
Am J Hematol; 1993 Apr; 42(4):367-74. PubMed ID: 8493987
[TBL] [Abstract][Full Text] [Related]
7. A novel case of Hb Phnom Penh: codons 117/118 (+ATC) as a cause of α+ -thalassemia.
Zhai YS; Tang HS; Zhou JY; Li DZ
Hemoglobin; 2012; 36(3):289-92. PubMed ID: 22432594
[TBL] [Abstract][Full Text] [Related]
8. Hb Graz or alpha 2 beta 2(2)(NA2)His-->Leu; a new beta chain variant observed in four families from southern Austria.
Liu JS; Molchanova TP; Gu LH; Wilson JB; Hopmeier P; Schnedl W; Balaun E; Krejs GJ; Huisman TH
Hemoglobin; 1992; 16(6):493-501. PubMed ID: 1487420
[TBL] [Abstract][Full Text] [Related]
9. Characterization of a new electrophoretically silent hemoglobin variant. Hb saale OR alpha 2beta 2 84(EF8)Thr --> Ala.
Bissé E; Zorn N; Heinrichs I; Eigel A; Van Dorsselaer A; Wieland H; Kister J; Marden MC
J Biol Chem; 2000 Jul; 275(28):21380-4. PubMed ID: 10770934
[TBL] [Abstract][Full Text] [Related]
10. Dominantly Inherited beta-Thalassemia.
Efremov GD
Hemoglobin; 2007; 31(2):193-207. PubMed ID: 17486503
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. Hb Adana or alpha 2(59)(E8)Gly-->Asp beta 2, a severely unstable alpha 1-globin variant, observed in combination with the -(alpha)20.5 Kb alpha-thal-1 deletion in two Turkish patients.
Cürük MA; Dimovski AJ; Baysal E; Gu LH; Kutlar F; Molchanova TP; Webber BB; Altay C; Gürgey A; Huisman TH
Am J Hematol; 1993 Dec; 44(4):270-5. PubMed ID: 8237999
[TBL] [Abstract][Full Text] [Related]
13. Hb Plasencia [α125(H8)Leu→Arg (α2)] is a frequent cause of α+-thalassemia in the Portuguese population.
Cunha E; Bento C; Oliveira A; Relvas L; Neves J; Gameiro M; Barros C; Araújo A; Macedo A; Rocha P; Costa R; Maia T; Ribeiro ML
Hemoglobin; 2013; 37(2):183-7. PubMed ID: 23368878
[TBL] [Abstract][Full Text] [Related]
14. A Novel Heme Pocket Hemoglobin Variant Associated with Normal Hematology: Hb Zara or α91(FG3)Leu→Ile (α2) (HBA2: c.274C > A).
Trova S; Mereu P; Decandia L; Cocco E; Masala B; Manca L; Pirastru M
Hemoglobin; 2015; 39(6):427-9. PubMed ID: 26291971
[TBL] [Abstract][Full Text] [Related]
15. Hemoglobin Montreal: a new variant with an extended beta chain due to a deletion of Asp, Gly, Leu at positions 73, 74, and 75, and an insertion of Ala, Arg, Cys, Gln at the same location.
Plaseska D; Dimovski AJ; Wilson JB; Webber BB; Hume HA; Huisman TH
Blood; 1991 Jan; 77(1):178-81. PubMed ID: 1845844
[TBL] [Abstract][Full Text] [Related]
16. Cord blood screening for alpha-thalassemia and hemoglobin variants by isoelectric focusing in northern Thai neonates: correlation with genotypes and hematologic parameters.
Charoenkwan P; Taweephol R; Sirichotiyakul S; Tantiprabha W; Sae-Tung R; Suanta S; Sakdasirisathaporn P; Sanguansermsri T
Blood Cells Mol Dis; 2010 Jun; 45(1):53-7. PubMed ID: 20299254
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. Novel interactions of two α-Hb variants with SEA deletion α
Srivorakun H; Singha K; Fucharoen G; Fucharoen S
Hematology; 2018 Apr; 23(3):187-191. PubMed ID: 28945175
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. Hemoglobin Birmingham and hemoglobin Galicia: two unstable beta chain variants characterized by small deletions and insertions.
Wilson JB; Webber BB; Hu H; Kutlar A; Kutlar F; Codrington JF; Prchal JT; Hall KM; de Pablos JM; Rodriguez I
Blood; 1990 May; 75(9):1883-7. PubMed ID: 2158827
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
