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Year : 2017 |
Volume: 4 |
Issue Number: 3 | Page: 110-113
CASE REPORT
A rare case of compound heterozygous B-thalassemia and hereditary persistence of fetal hemoglobin with Moya-Moya disease
Gupta Ashok, Mathur Priyanshu, Sharma Manish, Parmar Vimesh
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