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2. Hb Koya Dora [alpha142, Term-->Ser (TAA>TCA in alpha2)]: a rare mutation of the alpha2 gene stop codon associated with alpha-thalassemia. Brennan SO, Ryken S, Chan T. Hemoglobin; 2010; 34(4):402-5. PubMed ID: 20642339 [Abstract] [Full Text] [Related]
14. A heterozygote for Hb S beta, Hb C beta and Hb G Philadelphia beta in a family presenting evidence for heterogeneity of hemoglobin alpha chain loci. Rucknagel DL, Rising JA. Am J Med; 1975 Jul 10; 59(1):53-60. PubMed ID: 1138551 [Abstract] [Full Text] [Related]
15. Haemoglobin Q India (alpha 64(E13) aspartic acid histidine) associated with beta-thalassemia observed in three Sindhi families. Sukumaran PK, Merchant SM, Desai MP, Wiltshire BG, Lehmann H. J Med Genet; 1972 Dec 10; 9(4):436-42. PubMed ID: 4646552 [No Abstract] [Full Text] [Related]
16. [Hemoglobin Boumerdès alpha 2(37) (C2) Pro----Arg beta 2: a new variant of the alpha chain associated with hemoglobin S in an Algerian family]. Dahmane-Arbane M, Blouquit Y, Arous N, Bardakdjian J, Benamani M, Riou J, Benabadji M, Rosa J, Galacteros F. Nouv Rev Fr Hematol (1978); 1987 Dec 10; 29(5):317-20. PubMed ID: 3438164 [Abstract] [Full Text] [Related]
18. Identification of hemoglobin G-Philadelphia (alpha 68 Asn replaced by Lys) and hemoglobin Matsue-Oki (alpha 75 Asp replaced by Asn) in a black infant. Yi-Tao Z, Headlee ME, Henson J, Lam H, Wilson JB, Huisman TH. Biochim Biophys Acta; 1982 Oct 05; 707(2):206-12. PubMed ID: 6814490 [Abstract] [Full Text] [Related]