References
- TaherATWeatherallDJCappelliniMDThalassaemiaLancet20183911011615516728774421
- SankaranVGLettreGOrkinSHHirschhornJNModifier genes in Mendelian disorders: the example of hemoglobin disordersAnn N Y Acad Sci20101214475621039591
- WasiPPootrakulSPootrakulPPravatmuangPWinichagoonPFucharoenSThalassemia in ThailandAnn N Y Acad Sci19803443523636156628
- TheinSLWinichagoonPHeskethCThe molecular basis of beta-thalassemia in Thailand: application to prenatal diagnosisAm J Hum Genet19904733693752393018
- MaryamiFAzarkeivanAFallahMSZeinaliSA large cohort study of genotype and phenotype correlations of beta-thalassemia in Iranian populationInt J Hematol Oncol Stem Cell Res20159419820226865931
- SahuPKPatiSSMishraSKGenotype–phenotype correlation of beta-thalassemia spectrum of mutations in an Indian populationHematol Rep201242e922826799
- HoPJHallGWLuoLYWeatherallDJTheinSLBeta-thalassaemia intermedia: is it possible consistently to predict phenotype from genotype?Br J Haematol199810017089450794
- BhardwajUZhangYHLoreyFMcCabeLLMcCabeERMolecular genetic confirmatory testing from newborn screening samples for the common African-American, Asian Indian, Southeast Asian, and Chinese beta-thalassemia mutationsAm J Hematol200578424925515795925
- SirichotiyakulSSaetungRSanguansermsriTAnalysis of beta-thalassemia mutations in northern Thailand using an automated fluorescence DNA sequencing techniqueHemoglobin2003272899512779270
- SanguansermsriTPapeMLaigMHundrieserJFlatzGBeta zero-thalassemia in a Thai family is caused by a 3.4 kb deletion including the entire beta-globin geneHemoglobin19901421571682272839
- AsadovCAbdulalimovEMammadovaTGafarovaSGuliyevaYAliyevaGGenotype–phenotype correlations of beta-thalassemia mutations in an Azerbaijani populationTurk J Haematol201734325826328120779
- WeatherallDJThe challenge of haemoglobinopathies in resource-poor countriesBr J Haematol2011154673674421726207
- BoonyawatBMonsereenusornCTraivareeCMolecular analysis of beta-globin gene mutations among Thai beta-thalassemia children: results from a single center studyAppl Clin Genet2014725325825525381
- LaosombatVFucharoenSPPanichVMolecular basis of beta thalassemia in the south of ThailandAm J Hematol19924131941981415194
- LaosombatVWongchanchailertMSattayasevanaBWiriyasateinkulAFucharoenSClinical and hematological features of beta(+)-thalassemia (IVS-1 nt 5, G-C mutation) in Thai patientsEur J Haematol200167210010411722597
- ChengTCOrkinSHAntonarakisSEbeta-Thalassemia in Chinese: use of in vivo RNA analysis and oligonucleotide hybridization in systematic characterization of molecular defectsProc Natl Acad Sci U S A1984819282128256585831
- TreismanROrkinSHManiatisTSpecific transcription and RNA splicing defects in five cloned beta-thalassaemia genesNature198330259095915966188062
- OldJMKhanSNVermaIA multi-center study in order to further define the molecular basis of beta-thalassemia in Thailand, Pakistan, Sri Lanka, Mauritius, Syria, and India, and to develop a simple molecular diagnostic strategy by amplification refractory mutation system-polymerase chain reactionHemoglobin200125439740711791873