αthaiassemia in Thailand
The αthalassemia syndromes are remarkable both for their phenotypic diversity and for their different clinical severity. They are associated with variable degrees of αchain deficits; the clinical manifestations range from asymptomatic cases with normal hematologic findings to the totally lethal Hb B...
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th-mahidol.155162018-06-14T16:10:36Z αthaiassemia in Thailand P. Yinichagoon V. Thonglairuam S. Fucharoen V. S. Tanphaichito P. Wasi Mahidol University Biochemistry, Genetics and Molecular Biology Medicine The αthalassemia syndromes are remarkable both for their phenotypic diversity and for their different clinical severity. They are associated with variable degrees of αchain deficits; the clinical manifestations range from asymptomatic cases with normal hematologic findings to the totally lethal Hb Bart's hydrops fetalis syndrome. Recent molecular biology studies have clarified the defects in these αthalassemia syndromes around the world. This paper describes the αthalassemias in Thailand, and covers the types, molecular defects, incidence of each genotype, and their phenotypic expression. © 1988 Informa UK Ltd All rights reserved: reproduction in whole or part not permitted. 2018-06-14T09:06:39Z 2018-06-14T09:06:39Z 1988-01-01 Article Hemoglobin. Vol.12, No.5-6 (1988), 485-498 10.3109/03630268808991637 03630269 2-s2.0-0023698977 https://repository.li.mahidol.ac.th/handle/123456789/15516 Mahidol University SCOPUS https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=0023698977&origin=inward |
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Mahidol University |
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Mahidol University Library |
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Asia |
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Thailand Thailand |
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Mahidol University Institutional Repository |
| topic |
Biochemistry, Genetics and Molecular Biology Medicine |
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Biochemistry, Genetics and Molecular Biology Medicine P. Yinichagoon V. Thonglairuam S. Fucharoen V. S. Tanphaichito P. Wasi αthaiassemia in Thailand |
| description |
The αthalassemia syndromes are remarkable both for their phenotypic diversity and for their different clinical severity. They are associated with variable degrees of αchain deficits; the clinical manifestations range from asymptomatic cases with normal hematologic findings to the totally lethal Hb Bart's hydrops fetalis syndrome. Recent molecular biology studies have clarified the defects in these αthalassemia syndromes around the world. This paper describes the αthalassemias in Thailand, and covers the types, molecular defects, incidence of each genotype, and their phenotypic expression. © 1988 Informa UK Ltd All rights reserved: reproduction in whole or part not permitted. |
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Mahidol University |
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Mahidol University P. Yinichagoon V. Thonglairuam S. Fucharoen V. S. Tanphaichito P. Wasi |
| format |
Article |
| author |
P. Yinichagoon V. Thonglairuam S. Fucharoen V. S. Tanphaichito P. Wasi |
| author_sort |
P. Yinichagoon |
| title |
αthaiassemia in Thailand |
| title_short |
αthaiassemia in Thailand |
| title_full |
αthaiassemia in Thailand |
| title_fullStr |
αthaiassemia in Thailand |
| title_full_unstemmed |
αthaiassemia in Thailand |
| title_sort |
αthaiassemia in thailand |
| publishDate |
2018 |
| url |
https://repository.li.mahidol.ac.th/handle/123456789/15516 |
| _version_ |
1763493408359317504 |