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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
Year : 2017 | Volume: 4 | Issue Number: 3 | Page: 110-113
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