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.
4. 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]
5. Hb Montreal II: a novel elongated beta-globin variant caused by a frameshift mutation [beta142 (-C)]. Chagnon P; Mollica L; Belisle C; Deveaux C; Angelo GD; Roy DC; Soulières D; Busque L Hemoglobin; 2008; 32(4):351-9. PubMed ID: 18654885 [TBL] [Abstract][Full Text] [Related]
6. Hemoglobin Hammersmith [beta 42(CD1) Phe --> Ser] causing severe hemolytic anemia in a Japanese girl. Akiyama M; Murayama S; Yokoi K; Yanagisawa T; Hattori Y; Yamashiro Y; Eto Y; Fujisawa K Pediatr Blood Cancer; 2006 Nov; 47(6):839-41. PubMed ID: 16078214 [TBL] [Abstract][Full Text] [Related]
7. Hemoglobin Debrousse (beta 96[FG3]Leu-->Pro): a new unstable hemoglobin with twofold increased oxygen affinity. Lacan P; Kister J; Francina A; Souillet G; Galactéros F; Delaunay J; Wajcman H Am J Hematol; 1996 Apr; 51(4):276-81. PubMed ID: 8602627 [TBL] [Abstract][Full Text] [Related]
8. Globin chain synthesis in hemolytic anemia reticulocytes. A case of hemoglobin Burke. Suzuki H; Wada C; Kamata K; Takahashi E; Sato N; Kunitomo T Biochem Mol Biol Int; 1993 Jul; 30(3):425-31. PubMed ID: 8401300 [TBL] [Abstract][Full Text] [Related]
9. Two missense mutations in the beta-globin gene can cause severe beta thalassemia. Hemoglobin Medicine Lake (beta 32[B14]leucine-->glutamine; 98 [FG5] valine-->methionine). Coleman MB; Lu ZH; Smith CM; Adams JG; Harrell A; Plonczynski M; Steinberg MH J Clin Invest; 1995 Feb; 95(2):503-9. PubMed ID: 7860732 [TBL] [Abstract][Full Text] [Related]
10. 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]
11. Priapism following splenectomy in an unstable hemoglobin: hemoglobin Olmsted beta 141 (H19) Leu-->Arg. Thuret I; Bardakdjian J; Badens C; Wajcman H; Galacteros F; Vanuxem D; Perrimond H; Giraud F; Lena-Russo D Am J Hematol; 1996 Feb; 51(2):133-6. PubMed ID: 8579053 [TBL] [Abstract][Full Text] [Related]
12. Hb Alesha [beta67(E11)Val-->Met, GTG-->ATG] in an Argentinean girl. Eberle SE; Noguera NI; Sciuccati G; Bonduel M; Díaz L; Staciuk R; Targovnik HM; Feliu-Torres A Hemoglobin; 2007; 31(3):379-82. PubMed ID: 17654076 [TBL] [Abstract][Full Text] [Related]
13. Hb Southampton [beta106(G8)Leu-->Pro, CTG-->CCG] in an Argentinean boy. Eandi Eberle S; Noguera NI; Sciuccati G; Bonduel M; Díaz L; Staciuk R; Feliu-Torres A Hemoglobin; 2006; 30(3):401-3. PubMed ID: 16840233 [TBL] [Abstract][Full Text] [Related]
14. Hemoglobin Hakkari: an autosomal dominant form of beta thalassemia with inclusion bodies arising from de novo mutation in exon 2 of beta globin gene. Kanathezhath B; Hazard FK; Guo H; Kidd J; Azimi M; Kuypers FA; Vichinsky EP; Lal A Pediatr Blood Cancer; 2010 Feb; 54(2):332-5. PubMed ID: 19852066 [TBL] [Abstract][Full Text] [Related]
16. A dutch family with Hb Debrousse: severe anemia after parvovirus B19 infection. van Balen P; van Wijnen M; Hogeman PH; Wittebol S Hemoglobin; 2009; 33(3):269-73. PubMed ID: 19657843 [TBL] [Abstract][Full Text] [Related]
17. Hemoglobin sabine beta 91 (F 7) leu → pro. An unstable variant causing severe anemia with inclusion bodies. Schneider RG; Ueda S; Alperin JB; Brimhall B; Jones RT N Engl J Med; 1969 Apr; 280(14):739-45. PubMed ID: 5773354 [No Abstract] [Full Text] [Related]
18. 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]