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2. Double heterozygosity for Hb G-San Jose [beta7(A4)Glu-->Gly] and Hb Fukuoka [beta2(NA2)His-->Tyr] in a 2 1/2-year-old girl. Farah RA; Buchanan GR; Timmons CF; Phillips L; Fairbanks VF; Snow K; Hoyer JD Hemoglobin; 1999 Nov; 23(4):383-7. PubMed ID: 10569729 [No Abstract] [Full Text] [Related]
3. 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]
5. HB Taybe: description of genetics and laboratory findings in an Israeli Arab family. Ben-Bassat I; Simjanovska L; Jaber L; Efremov GD Hemoglobin; 1998 Mar; 22(2):161-6. PubMed ID: 9576334 [No Abstract] [Full Text] [Related]
6. Hb Sun Prairie or alpha(2)130(H13)Ala----Pro beta 2; second observation in an Indian adult. Plaseska D; Gu LH; Wilson JB; Codrington JF; Huisman TH; Dash S Hemoglobin; 1990; 14(5):491-7. PubMed ID: 2079431 [No Abstract] [Full Text] [Related]
7. Identification of Hb Zürich [alpha 2 beta 2(63)(E7)His-->Arg] by DNA analysis in a Brazilian family. Miranda SR; Kimura EM; Saad ST; Costa FF Hemoglobin; 1994 Sep; 18(4-5):337-41. PubMed ID: 7852089 [No Abstract] [Full Text] [Related]
8. Compound heterozygosity for Hb S [β6(A3)Glu→Val] and Hb Kenya (Aγ81Leu-β86Ala) in a Ugandan woman. Han ZJ; Lapuz C; Rovenger JF; Dreyfus PA; Vispo BG; Ou CN; Luo HY; Chui DH; Gallivan MV Hemoglobin; 2012; 36(3):270-5. PubMed ID: 22384817 [TBL] [Abstract][Full Text] [Related]
9. Hb Madrid [beta115(G17)Ala-->Pro] in a Korean family with chronic hemolytic anemia. Kim JY; Park SS; Jung HL; Keum DH; Park H; Chang YH; Lee YJ; Cho HI Hemoglobin; 2000 May; 24(2):133-8. PubMed ID: 10870884 [TBL] [Abstract][Full Text] [Related]
10. Hb Castilla [beta32(B14)Leu --> Arg] caused by a de novo mutation. Walker L; McFarlane A; Patterson M; Eng B; Waye JS Hemoglobin; 2003 Nov; 27(4):253-6. PubMed ID: 14649317 [No Abstract] [Full Text] [Related]
11. Hb K-Ibadan [beta 46(CD5)Gly----Glu] in an Italian family. Castagnola M; Cassiano L; Rossetti DV; Marucci L; Ferro A; Scarano C; Monaco M; Celozzi AM Hemoglobin; 1990; 14(6):647-51. PubMed ID: 1983219 [No Abstract] [Full Text] [Related]
12. Characterization of Hb Volga [beta 27(B9)Ala-->Asp] and Hb J-Wenchang-Wuming [alpha 11(A9)Lys-->Gln] in the population of the United States. Wang WC; Carter H; Choitz HC; Hall R; Hine TK; Jue DL; Moo-Penn WF Hemoglobin; 1993 Feb; 17(1):67-71. PubMed ID: 8454471 [No Abstract] [Full Text] [Related]
13. Hb Saint Etienne or Hb Istanbul [beta92(F8)His-->Gln] found in an Argentinean family. de Weinstein BI; Plaseska-Karanfilska D; Efremov GD Hemoglobin; 2000 May; 24(2):149-52. PubMed ID: 10870887 [No Abstract] [Full Text] [Related]
14. The clinical and laboratory spectrum of Hb C [β6(A3)Glu→Lys, GAG>AAG] disease. Cook CM; Smeltzer MP; Mortier NA; Kirk SE; Despotovic JM; Ware RE; Hankins JS Hemoglobin; 2013; 37(1):16-25. PubMed ID: 23297836 [TBL] [Abstract][Full Text] [Related]
15. Hb Fairfax [HBB:c.285_286insGAGCTGCACTGTGAC] in a Brazilian patient with severe hemolytic anemia-identification and functional study. Jorge SE; Lanaro C; Albuquerque DM; Nascimento PH; Pedroso GA; Oliveira SC; Grigoleto MRP; Santos MNN; Costa FF; Sonati MF Ann Hematol; 2019 Sep; 98(9):2253-2255. PubMed ID: 31253996 [No Abstract] [Full Text] [Related]
16. [Hemoglobin E (26 Glu-Lys) and beta-thalassemia in a Mexican family]. Bergés-García A; del Angel-Guevara O; Ruiz-Reyes G; Dorantes-Mesa S; Ibarra B; de Ruiz NL; de Kuttel VF Bol Med Hosp Infant Mex; 1984 Apr; 41(4):205-10. PubMed ID: 6466420 [No Abstract] [Full Text] [Related]
17. Hb Tak confirmed by DNA analysis: not expressed as thalassemia in a Hb Tak/Hb E compound heterozygote. Hoyer JD; Wick MJ; Thibodeau SN; Viker KA; Conner R; Fairbanks VF Hemoglobin; 1998 Jan; 22(1):45-52. PubMed ID: 9494047 [TBL] [Abstract][Full Text] [Related]
18. Strategy for identification by mass spectrometry of a new human hemoglobin variant with two mutations in Cis in the beta-globin chain: Hb S-Clichy [beta6(A3)Glu-->Val; beta8(A5)Lys-->Thr]. Zanella-Cleon I; Préhu C; Joly P; Riou J; Becchi M; Wajcman H; Francina A Hemoglobin; 2009; 33(3):177-87. PubMed ID: 19657831 [TBL] [Abstract][Full Text] [Related]
19. Compound heterozygosity for two alpha-globin gene defects, Hb Taybe (alpha 1; 38 or 39 minus Thr) and a poly A mutation (alpha 2; AATAAA-->AATAAG), results in a severe hemolytic anemia. Pobedimskaya DD; Molchanova TP; Streichman S; Huisman TH Am J Hematol; 1994 Nov; 47(3):198-202. PubMed ID: 7942784 [TBL] [Abstract][Full Text] [Related]
20. Homozygous Hb Sallanches [alpha104(G11)Cys-->Tyr] in a Pakistani child with Hb H disease. Waye JS; Walker L; Chui DH; Lafferty J; Kirby M Hemoglobin; 2000 Nov; 24(4):355-7. PubMed ID: 11186268 [No Abstract] [Full Text] [Related] [Next] [New Search]