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25. [Association of Hb Lepore Boston and beta-+ thalassemia in a Spanish family]. Romero C; Fernández Fuertes I; Hernández Jodra M; Navarro JL Sangre (Barc); 1983; 28(3):348-52. PubMed ID: 6623295 [No Abstract] [Full Text] [Related]
26. Compound heterozygosity of Hb D(Iran) (beta(22) Glu-->Gln) and beta(0)-thalassemia (619 bp-deletion) in India. Agrawal MG; Bhanushali AA; Dedhia P; Jeswani KD; Dayanand S; Dasgupta A; Das BR Eur J Haematol; 2007 Sep; 79(3):248-50. PubMed ID: 17655708 [TBL] [Abstract][Full Text] [Related]
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29. Hb Grove City [β38(C4)Thr→Ser, ACC>AGC; HBB: c.116C>G]: a new low oxygen affinity β chain variant. Taliercio RM; Ashton RW; Horwitz L; Swanson KC; Wendt PC; Hoyer JD; Oliveira JL Hemoglobin; 2013; 37(4):396-403. PubMed ID: 23651408 [TBL] [Abstract][Full Text] [Related]
30. Genetic heterogeneity of thalassemias in Mexican mestizo patients with hemolytic anemia. Ibarra B; Vaca G; de la Mora E; Romero F; Aguilar-Luna C; Mejía A; Esparza MA; Pérez G; Ornelas ML; Cantú JM Hum Hered; 1988; 38(2):95-100. PubMed ID: 2454217 [TBL] [Abstract][Full Text] [Related]
31. Ten Years of Routine α- and β-Globin Gene Sequencing in UK Hemoglobinopathy Referrals Reveals 60 Novel Mutations. Henderson SJ; Timbs AT; McCarthy J; Gallienne AE; Proven M; Rugless MJ; Lopez H; Eglinton J; Dziedzic D; Beardsall M; Khalil MS; Old JM Hemoglobin; 2016; 40(2):75-84. PubMed ID: 26635043 [TBL] [Abstract][Full Text] [Related]
32. DNA-polymorphic patterns linked to the beta-globin genes in German families affected with hemoglobinopathies and thalassemias: a comparison to other ethnic groups. Oehme R; Kohne E; Horst J Hum Genet; 1985; 71(3):219-22. PubMed ID: 2998970 [TBL] [Abstract][Full Text] [Related]
33. Hemoglobin E diseases: hematological, analytical, and biosynthetic studies in homozygotes and double heterozygotes for alpha-thalassemia. Wong SC; Ali MA Am J Hematol; 1982 Aug; 13(1):15-21. PubMed ID: 7137163 [TBL] [Abstract][Full Text] [Related]
34. Post-translational control of human hemoglobin synthesis: the role of the differential affinity between globin chains in the control of mutated globin gene expression. Mavilio F; Marinucci M; Guerriero R; Cappellozza G; Tentori L Biochim Biophys Acta; 1980 Dec; 610(2):339-51. PubMed ID: 7213630 [TBL] [Abstract][Full Text] [Related]
35. Laboratory investigation of hemoglobinopathies and thalassemias: review and update. Clarke GM; Higgins TN Clin Chem; 2000 Aug; 46(8 Pt 2):1284-90. PubMed ID: 10926923 [TBL] [Abstract][Full Text] [Related]
36. Hemoglobin Evanston: alpha 14(A12) Trp leads to Arg. A variant hemoglobin associated with alpha-thalassemia-2. Moo-Penn WF; Baine RM; Jue DL; Johnson MH; McGuffey JE; Benson JM Biochim Biophys Acta; 1983 Sep; 747(1-2):65-70. PubMed ID: 6882779 [TBL] [Abstract][Full Text] [Related]
37. Hb Washtenaw [ beta 11(A8)Val-->Phe]: an electrophorectically silent, unstable, low oxygen affinity variant associated with anemia and chronic cyanosis. Krishnan K; Martinez F; Wille RT; Jones RT; Shih DT; Head C; Fairbanks VF; Dabich L Hemoglobin; 1994 Sep; 18(4-5):285-95. PubMed ID: 7852083 [TBL] [Abstract][Full Text] [Related]