Cogent Medicine
 2019
DOI: 10.1080/2331205x.2019.1581448
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A compound heterozygous −29 A>G and IVS-I-1 G>A mutation of HBB gene leading to β-thalassemia intermedia in a Syrian patient: A case report

Hossam Murad
1
,
Faten Moassas
2
,
Bashar Ali
3
et al.
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