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...
Saved in:
Main Authors: | P. Yinichagoon, V. Thonglairuam, S. Fucharoen, V. S. Tanphaichito, P. Wasi |
---|---|
Other Authors: | Mahidol University |
Format: | Article |
Published: |
2018
|
Subjects: | |
Online Access: | https://repository.li.mahidol.ac.th/handle/123456789/15516 |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Institution: | Mahidol University |
Similar Items
-
The molecular basis of AE-bart's disease
by: V. Thonglairuam, et al.
Published: (2018) -
βthalassemia associated with αthalassemia in Thailand
by: S. Fucharoen, et al.
Published: (2018) -
Immunologic diagnosis of αthalassemia traits
by: P. Wasi, et al.
Published: (2018) -
Hemoglobin Thailand [α 56 (e 5) lys→thr]: A new abnormal human hemoglobin
by: S. Pootrakul, et al.
Published: (2018) -
Two cases of compound heterozygosity for Hb Hekinan [α27(B8)Glu→ Asp (α1)] and α-thalassemia in Thailand
by: Lukana Ngiwsara, et al.
Published: (2018)