Detalhe da pesquisa
1.
Essential genetic modifiers and their measurable impact in a community-recruited population analysis for non-severe hemoglobin E/ß-thalassemia prenatal genetic counseling.
Blood Cells Mol Dis
; 103: 102765, 2023 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-37353362
2.
Lessons learned from a prenatal diagnosis program for thalassemia in Thailand.
Prenat Diagn
; 40(8): 998-1004, 2020 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-32356374
3.
Frequency of hemoglobin E/ß-thalassemia compound heterozygotes with low hemoglobin F phenotype among cases with a diagnosis of hemoglobin E homozygote, determined by high-performance liquid chromatography, in prenatal control program for ß-thalassemia.
Ann Hematol
; 96(10): 1763-1765, 2017 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-28803407
4.
Evaluation of a cryopreservation procedure to set up a new bone marrow transplant unit using lymphocyte proliferation test.
Immunol Invest
; 41(1): 97-103, 2012.
Artigo
em Inglês
| MEDLINE | ID: mdl-21649473
5.
Q Sepharose micro-column chromatography: A simple screening method for identifying beta thalassemia traits and hemoglobin E carriers.
Clin Biochem
; 49(16-17): 1288-1291, 2016 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-27399165
6.
A blood transfusion leading to misdiagnosis of beta-thalassaemia carrier status.
Blood Transfus
; 8(1): 69-70, 2010 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-20104282