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7. An alpha-thalassemic hemoglobinopathy: homozygosity for the HB Agrinio alpha 2-globin chain variant. Traeger-Synodinos J, Metaxotou-Mavromati A, Kanavakis E, Vrettou C, Papassotiriou I, Michael T, Kattamis C. Hemoglobin; 1998 May; 22(3):209-15. PubMed ID: 9629496 [Abstract] [Full Text] [Related]
8. Haemoglobin Tunis-Bizerte: a new alpha 1 globin 129 Leu-->Pro unstable variant with thalassaemic phenotype. Darbellay R, Mach-Pascual S, Rose K, Graf J, Beris P. Br J Haematol; 1995 May; 90(1):71-6. PubMed ID: 7786798 [Abstract] [Full Text] [Related]
18. A case of hemoglobin Indianapolis [beta 112(G14) Cys----Arg] in an individual from Cordoba, Spain. Baiget M, Gomez Pereira C, Jue DL, Johnson MH, McGuffey JE, Moo-Penn WF. Hemoglobin; 1986 Aug; 10(5):483-94. PubMed ID: 3781865 [Abstract] [Full Text] [Related]
19. 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 Aug; 33(3):177-87. PubMed ID: 19657831 [Abstract] [Full Text] [Related]