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12. Hb Capa or alpha (2)94(G1)Asp-->Gly beta 2, a mildly unstable variant with an A-->G (GAC-->GGC) mutation in codon 94 of the alpha 1-globin gene. Dinçol G; Dinçol K; Erdem S; Pobedimskaya DD; Molchanova TP; Ye Z; Webber BB; Wilson JB; Huisman TH Hemoglobin; 1994 Jan; 18(1):57-60. PubMed ID: 8195009 [No Abstract] [Full Text] [Related]
13. Two new hemoglobin variants: Hb Brem-sur-Mer [beta9(A6)Ser-->Tyr] and Hb Passy [alpha81(F2)Ser-->Pro (alpha2)]. Lacan P; Moreau M; Becchi M; Zanella-Cleon I; Aubry M; Louis JJ; Couprie N; Francina A Hemoglobin; 2005; 29(1):69-75. PubMed ID: 15768558 [TBL] [Abstract][Full Text] [Related]
14. Identification of Mutations Causing Aberrant Termination and Deficient Splice Donor Site on the HBA1 Gene. Farashi S; Vakili S; Garous NF; Ashki M; Forouzesh Pour F; Zeinali F; Rad F; Imanian H; Azarkeivan A; Najmabadi H Hemoglobin; 2016; 40(1):38-43. PubMed ID: 26531168 [TBL] [Abstract][Full Text] [Related]
15. [Hemoglobin D Punjab in Dagestan]. Khasaev ASh; Shamov IA; Kulagin MN; Kolodeĭ SV; Spivak VA Gematol Transfuziol; 1983 Jun; 28(6):47-8. PubMed ID: 6884742 [No Abstract] [Full Text] [Related]
16. Compound heterozygosity for Hb Spanish town [alpha27(B8)Glu-->Val], Hb S [beta6(A3)Glu-->Val] and the -alpha(3.7kb) thalassemia deletion. Faustino P; Picanço I; Miranda A; Seixas T; Ferrão A; Morais A; Lavinha J; Romão L Hemoglobin; 2002 May; 26(2):185-9. PubMed ID: 12144063 [No Abstract] [Full Text] [Related]
17. Hb Fulton-Georgia [α20(B1)His→Pro; HBA1: c.62A>C]: a new α-globin variant coinherited with α-thalassemia-2 (3.7 kb deletion) and Hb SC disease. Zhuang L; Patel N; Bryant S; Kutlar A; Kutlar F; Young AN Hemoglobin; 2013; 37(5):481-5. PubMed ID: 24006930 [TBL] [Abstract][Full Text] [Related]