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3. Heterogeneity and origins of the alpha-thalassemias. Weatherall DJ; Higgs DR; Clegg JB; Hill AS; Nicholls R Birth Defects Orig Artic Ser; 1987; 23(5A):3-14. PubMed ID: 3689911 [TBL] [Abstract][Full Text] [Related]
4. The relationship between the common mutations of the alpha gene cluster and its evolutionary history. Weatherall DJ; Higgs DR; Clegg JB; Hill AS; Nicholls R; Wainscoat JS Prog Clin Biol Res; 1986; 218():47-62. PubMed ID: 3763644 [TBL] [Abstract][Full Text] [Related]
5. The genetics of thalassemia. Bank A Schweiz Med Wochenschr; 1983 Oct; 113(40):1415-9. PubMed ID: 6316485 [TBL] [Abstract][Full Text] [Related]
6. Molecular pathology of alpha-thalassemia. Liebhaber SA; Kan YW Birth Defects Orig Artic Ser; 1982; 18(7):35-44. PubMed ID: 6760927 [No Abstract] [Full Text] [Related]
7. Polymorphism and molecular pathology of the human beta-globin gene. Orkin SH; Antonarakis SE; Kazazian HH Prog Hematol; 1983; 13():49-73. PubMed ID: 6366914 [No Abstract] [Full Text] [Related]
9. [Thalassemia intermedia caused by interaction of IVS-1 1(G--A) mutation in the beta-globin gene and heterozygotic triplication in the alpha-globin gene]. Martínez-López J; Galán García P; del Río E; Baiget M; Gilsanz Rodríguez F Rev Clin Esp; 1998 Mar; 198(3):153-5. PubMed ID: 9586437 [TBL] [Abstract][Full Text] [Related]
10. [Molecular diagnosis in a Korean family with thalassemia intermedia due to co-inheritance of triplicated alpha-globin genes (alphaalpha/alphaalphaalpha(anti 3.7)) and beta-thalassemia trait (IVS-II-1 G-->A)]. Chen M; Han JY; Sun Q; Kim IH; Ren Z; Huang S; Zeng Y Zhonghua Xue Ye Xue Za Zhi; 2000 Apr; 21(4):195-7. PubMed ID: 11876981 [TBL] [Abstract][Full Text] [Related]
11. Use of haplotype analysis in the beta-globin gene cluster to discover beta-thalassemia mutations. Kazazian HH; Antonarakis SE; Cheng T; Boehm CD; Waber PG Prog Clin Biol Res; 1983; 134():91-8. PubMed ID: 6665005 [TBL] [Abstract][Full Text] [Related]
12. Molecular characterization of beta-thalassemia major and beta-thalassemia intermedia in China and Southeast Asia. Kazazian HH; Dowling CE; Waber PG; Huang SZ; Lo WH; Li A; Tam JW; Kang J; Antonarakis SE Prog Clin Biol Res; 1987; 251():401-12. PubMed ID: 3432272 [TBL] [Abstract][Full Text] [Related]
14. "Silent" nucleotide substitution in codon 24 of a beta+ thalassemia globin gene activates splice site in coding sequence RNA. Humphries RK; Ley T; Goldsmith ME; Kantor JA; Cline AC; Nienhuis AW Prog Clin Biol Res; 1983; 134():123-6. PubMed ID: 6664994 [TBL] [Abstract][Full Text] [Related]
15. Distinct phenotypic expression associated with a new hyperunstable alpha globin variant (Hb heraklion, alpha1cd37(C2)Pro>0): comparison to other alpha-thalassemic hemoglobinopathies. Traeger-Synodinos J; Papassotiriou I; Metaxotou-Mavrommati A; Vrettou C; Stamoulakatou A; Kanavakis E Blood Cells Mol Dis; 2000 Aug; 26(4):276-84. PubMed ID: 11042028 [TBL] [Abstract][Full Text] [Related]
16. [Moleculo-genetic study of beta-thalassemia heterogenity in the USSR]. Dergunova LV; Mazurova OL; Slominskiĭ PA; Limborskaia SA Vopr Med Khim; 1983; 29(3):33-8. PubMed ID: 6308904 [TBL] [Abstract][Full Text] [Related]
17. [The molecular basis of dominantly inherited beta-thalassemia]. Faustino P; Barbot J; Gonçalves J; Peres MJ; Lavinha J Acta Med Port; 1999; 12(7-11):293-6. PubMed ID: 10707468 [TBL] [Abstract][Full Text] [Related]
18. The phenotypic diversity of monogenic disease: lessons from the thalassemias. Weatherall DJ Harvey Lect; 1998-1999; 94():1-20. PubMed ID: 11070950 [TBL] [Abstract][Full Text] [Related]