References
- TaherATWeatherallDJCappelliniMDThalassaemiaLancet20183911011615516728774421
- FucharoenSViprakasitVHb H disease: clinical course and disease modifiersHematology2009200912634
- ChuiDHFucharoenSChanVHemoglobin H disease: not necessarily a benign disorderBlood2003101379180012393486
- OrigaRBarellaSPagliettiMEHematological phenotypes in children according to the alpha-globin genotypesBlood Cells Mol Dis20176910210629162392
- NuinoonMJeenduangNKesornsitAHorpetDPlyduangTHematological and molecular characterization of a novel Hb A2 variant with homozygous alpha-thalassemia-2 in a Southern Thai individualHemoglobin201741321321528795619
- CharoenkwanPWanapirakCThanarattanakornPHemoglobin E levels in double heterozygotes of hemoglobin E and SEA-type alpha-thalassemiaSoutheast Asian J Trop Med Public Health200536246747015916057
- ChongSSBoehmCDHiggsDRCuttingGRSingle-tube multiplex-PCR screen for common deletional determinants of alpha-thalassemiaBlood200095136036210607725
- BoonyawatBPhotiaAMonsereenusornCRujkijyanontPTraivareeCMolecular characterization of Hb H and AEBart’s diseases in Thai children: Phramongkutklao Hospital experiencesJ Med Assoc Thai20171002167174
- BoonsaSSanchaisuriyaKFucharoenGWiangnonSJetsrisuparbAFucharoenSThe diverse molecular basis and hematological features of Hb H and AE Bart’s diseases in Northeast ThailandActa Haematol2004111314915415034236
- ChanVChanVWTangMLauKToddDChanTKMolecular defects in Hb H hydrops fetalisBr J Haematol19979622242289029003
- WasiPNa-NakornSPootrakulPPanichVIncidence of haemoglobin Thai: a re-examination of the genetics of alpha-thalassaemic diseasesAnn Hum Genet19723544674704672504
- LalAGoldrichMLHainesDAAzimiMSingerSTVichinskyEPHeterogeneity of hemoglobin H disease in childhoodN Engl J Med2011364871071821345100
- FucharoenSWinichagoonPPootrakulPPiankijagumAWasiPDifferences between two types of Hb H disease, alpha-thalassemia 1/ alpha-thalassemia 2 and alpha-thalassemia 1/Hb constant springBirth Defects Orig Artic Ser1987235A3093153689912
- NguyenVHSanchaisuriyaKWongprachumKHemoglobin Constant Spring is markedly high in women of an ethnic minority group in Vietnam: a community-based survey and hematologic featuresBlood Cells Mol Dis201452416116524368026
- CaiRLiLLiangXPrevalence survey and molecular characterization of alpha and beta thalassemia in Liuzhou city of GuangxiZhonghua Liu Xing Bing Xue Za Zhi200223428128512411074
- ViprakasitVEkwattanakitSChalaowNClinical presentation and molecular identification of four uncommon alpha globin variants in Thailand. Initiation codon mutation of alpha2-globin Gene (HBA2:c.1delA), donor splice site mutation of alpha1-globin gene (IVSI-1, HBA1:c.95 + 1G>A), hemoglobin Queens Park/Chao Pra Ya (HBA1:c.98T>A) and hemoglobin Westmead (HBA2:c.369C>G)Acta Haematol20141312889424081251
- ViprakasitVTyanPRodmaiSTaherATIdentification and key management of non-transfusion-dependent thalassaemia patients: not a rare but potentially under-recognised conditionOrphanet J Rare Dis2014913125265971
- BowdenDKHillAVHiggsDROppenheimerSJWeatherallDJCleggJBDifferent hematologic phenotypes are associated with the leftward (-alpha 4.2) and rightward (-alpha 3.7) alpha+-thalassemia deletionsJ Clin Invest198779139433793931
- LaosombatVViprakasitVChotsampancharoenTClinical features and molecular analysis in Thai patients with HbH diseaseAnn Hematol200988121185119219390853
- SripichaiOMakarasaraWMunkongdeeTA scoring system for the classification of beta-thalassemia/Hb E disease severityAm J Hematol200883648248418186524
- FucharoenSWinichagoonPPrayoonwiwatWPootrakulPPiankijagumAWasiPClinical and hematologic manifestations of AE Bart diseaseBirth Defects Orig Artic Ser1987235A3273323689914
- GalanelloRMelisMAPagliettiECornacchiaGde VirgiliisSCaoASerum ferritin levels in hemoglobin H diseaseActa Haematol198369156586401895
- ChenFEOoiCHaSYGenetic and clinical features of hemoglobin H disease in Chinese patientsN Engl J Med2000343854455010954762