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2. Molecular genetics of human hemoglobin synthesis. Forget BG Ann Intern Med; 1979 Oct; 91(4):605-16. PubMed ID: 384860 [TBL] [Abstract][Full Text] [Related]
3. A spontaneous mutation produced a novel elongated beta-globin chain structural variant (Hb Agnana) with a thalassemia-like phenotype. Ristaldi MS; Pirastu M; Murru S; Casula L; Loudianos G; Cao A; Sciarratta GV; Agosti S; Parodi MI; Leone D Blood; 1990 Mar; 75(6):1378-9. PubMed ID: 2310835 [No Abstract] [Full Text] [Related]
4. Structure of human hemoglobin messenger RNA and its relation to hemoglobinopathies. Wilson JT; Marotta CA; Forget BG; Weissman SM Trans Assoc Am Physicians; 1977; 90():117-26. PubMed ID: 205979 [TBL] [Abstract][Full Text] [Related]
5. A substitution of cytosine for thymine in codon 110 of the human beta-globin gene is a novel cause of beta-thalassemia phenotypes. Naritomi Y; Naito Y; Nakashima H; Yokota E; Imamura T Hum Genet; 1988 Sep; 80(1):11-5. PubMed ID: 3417300 [TBL] [Abstract][Full Text] [Related]
6. Hb Filottrano [codon 120 (-A)]: a novel frameshift mutation in exon 3 of the β-globin gene causing dominantly inherited β-thalassemia intermedia. Amato A; Cappabianca MP; Perri M; Zaghis I; Mastropietro F; Ponzini D; Di Biagio P; Piscitelli R Hemoglobin; 2012; 36(5):480-4. PubMed ID: 22992010 [TBL] [Abstract][Full Text] [Related]
7. A single nucleotide deletion in codon 123 of the beta-globin gene causes an inclusion body beta-thalassaemia trait: a novel elongated globin chain beta Makabe. Fucharoen S; Kobayashi Y; Fucharoen G; Ohba Y; Miyazono K; Fukumaki Y; Takaku F Br J Haematol; 1990 Jul; 75(3):393-9. PubMed ID: 2167124 [TBL] [Abstract][Full Text] [Related]
8. Hb Questembert is due to a base substitution (T-->C) in codon 131 of the alpha 2-globin gene and has an alpha-thalassemia biosynthetic ratio. Rochette J; Barnetson R; Thein SL; Varet B; Valensi F Am J Hematol; 1995 Apr; 48(4):289-90. PubMed ID: 7717382 [No Abstract] [Full Text] [Related]
12. The alpha-chain-termination mutants and their relation to the alpha-thalassaemias. Weatherall DJ; Clegg JB Philos Trans R Soc Lond B Biol Sci; 1975 Aug; 271(913):411-55. PubMed ID: 240178 [TBL] [Abstract][Full Text] [Related]
13. 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]
14. Molecular genetics of human hemoglobin. Weatherall DJ; Clegg JB Annu Rev Genet; 1976; 10():157-78. PubMed ID: 797307 [No Abstract] [Full Text] [Related]
17. The alpha / beta and alpha 2 / alpha 1-globin mRNA ratios in different forms of alpha-thalassemia. Smetanina NS; Leonova JY; Levy N; Huisman TH Biochim Biophys Acta; 1996 Apr; 1315(3):188-92. PubMed ID: 8611658 [TBL] [Abstract][Full Text] [Related]
18. Hemoglobin M Iwate is caused by a C----T transition in codon 87 of the human alpha 1-globin gene. Horst J; Assum G; Griese EU; Eigel A; Hampl W; Kohne E Hum Genet; 1987 Jan; 75(1):53-5. PubMed ID: 3026948 [TBL] [Abstract][Full Text] [Related]
19. Molecular basis of beta (0)-thalassemia/HbE disease in Thailand. Petmitr S; Wilairat P; Kownkon J; Winichagoon P; Fucharoen S Biochem Biophys Res Commun; 1989 Jul; 162(2):846-51. PubMed ID: 2757643 [TBL] [Abstract][Full Text] [Related]
20. -Thalassaemia due to a structural haemoglobin variant. Weatherall DJ; Clegg JB Biochimie; 1972; 54(5):665-7. PubMed ID: 4654163 [No Abstract] [Full Text] [Related] [Next] [New Search]