एपीए उद्धरण

Dharmadhikari, A. V., Ghosh, R., Yuan, B., Liu, P., Dai, H., Al Masri, S., . . . Bi, W. (2019). Copy number variant and runs of homozygosity detection by microarrays enabled more precise molecular diagnoses in 11,020 clinical exome cases. Genome Med.

शिकागो स्टाइल उद्धरण

Dharmadhikari, Avinash V., et al. "Copy Number Variant and Runs of Homozygosity Detection By Microarrays Enabled More Precise Molecular Diagnoses in 11,020 Clinical Exome Cases." Genome Med 2019.

एमएलए उद्धरण

Dharmadhikari, Avinash V., et al. "Copy Number Variant and Runs of Homozygosity Detection By Microarrays Enabled More Precise Molecular Diagnoses in 11,020 Clinical Exome Cases." Genome Med 2019.