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NGS-based expanded carrier screening for genetic disorders in North Indian population reveals unexpected results – a pilot study
BMC medical genetics, Vol. 21, Issue 1, Pages 216, 2020
PMID: 33138774
To determine the carrier frequency and pathogenic variants of common genetic disorders in the north Indian population by using next generation sequencing (NGS).
https://www.ncbi.nlm.nih.gov/pubmed/33138774
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