| dc.contributor.author |
Jomoui W. |
|
| dc.contributor.author |
Tepakhan W. |
|
| dc.date.accessioned |
2022-03-10T13:16:38Z |
|
| dc.date.available |
2022-03-10T13:16:38Z |
|
| dc.date.issued |
2021 |
|
| dc.identifier.issn |
17515521 |
|
| dc.identifier.other |
2-s2.0-85102624459 |
|
| dc.identifier.uri |
https://ir.swu.ac.th/jspui/handle/123456789/17230 |
|
| dc.identifier.uri |
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85102624459&doi=10.1111%2fijlh.13511&partnerID=40&md5=97dbaf0e7f6fbb8f1c75d0b3b6da73b1 |
|
| dc.description.abstract |
[No abstract available] |
|
| dc.language |
en |
|
| dc.subject |
hemoglobin |
|
| dc.subject |
hemoglobin beta chain |
|
| dc.subject |
hemoglobin beta chain |
|
| dc.subject |
hemoglobin F |
|
| dc.subject |
hemoglobin variant |
|
| dc.subject |
adult |
|
| dc.subject |
agar gel electrophoresis |
|
| dc.subject |
allele |
|
| dc.subject |
alpha thalassemia |
|
| dc.subject |
BCL11A gene |
|
| dc.subject |
beta thalassemia |
|
| dc.subject |
blood sampling |
|
| dc.subject |
capillary electrophoresis |
|
| dc.subject |
case report |
|
| dc.subject |
clinical article |
|
| dc.subject |
disease classification |
|
| dc.subject |
DNA sequencing |
|
| dc.subject |
gene |
|
| dc.subject |
gene deletion |
|
| dc.subject |
gene mutation |
|
| dc.subject |
HBS1L MYB gene |
|
| dc.subject |
hematology |
|
| dc.subject |
hemoglobin blood level |
|
| dc.subject |
heterozygote |
|
| dc.subject |
human |
|
| dc.subject |
KLF1 gene |
|
| dc.subject |
Letter |
|
| dc.subject |
male |
|
| dc.subject |
multiplex polymerase chain reaction |
|
| dc.subject |
pathogenesis |
|
| dc.subject |
phenotype |
|
| dc.subject |
prediction |
|
| dc.subject |
prevalence |
|
| dc.subject |
protein expression |
|
| dc.subject |
single nucleotide polymorphism |
|
| dc.subject |
Thailand |
|
| dc.subject |
ultraviolet radiation |
|
| dc.subject |
beta thalassemia |
|
| dc.subject |
genetics |
|
| dc.subject |
beta-Globins |
|
| dc.subject |
beta-Thalassemia |
|
| dc.subject |
Fetal Hemoglobin |
|
| dc.subject |
Hemoglobins, Abnormal |
|
| dc.subject |
Heterozygote |
|
| dc.subject |
Humans |
|
| dc.subject |
Sequence Deletion |
|
| dc.title |
Characterization and identification of Prachinburi β0-thalassemia: A novel-60 kb deletion in beta globin gene related to high levels of Hb F in heterozygous state |
|
| dc.type |
Letter |
|
| dc.rights.holder |
Scopus |
|
| dc.identifier.bibliograpycitation |
International Journal of Laboratory Hematology. Vol 43, No.4 (2021), p.O200-O203 |
|
| dc.identifier.doi |
10.1111/ijlh.13511 |
|