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1.
A Case of Misdiagnosis Caused by the Coinheritance of Hb G-Siriraj [ß7(A4)GluâLys; HBB: c.22G>A] and Hb H Disease.
Hemoglobin
; 46(6): 338-340, 2022 Nov.
Artículo
en Inglés
| MEDLINE | ID: mdl-36691989
2.
[Association Analysis between Genotype and Phenotype of α,ß-Thalassaemia Carriers in Huizhou Area of Guangdong Province].
Zhongguo Shi Yan Xue Ye Xue Za Zhi
; 31(4): 1133-1137, 2023 Aug.
Artículo
en Zh
| MEDLINE | ID: mdl-37551488
3.
Genetic counseling and prenatal decision for hemoglobin H disease caused by the rare α2 codon 30 (-GAG) (HBA2: c.91_93delGAG) mutation and the SEA deletion: Case series study.
Taiwan J Obstet Gynecol
; 60(4): 763-765, 2021 Jul.
Artículo
en Inglés
| MEDLINE | ID: mdl-34247821
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