Author

Niladri Sekhar Bhunia

All India Institute of Medical Sciences, KalyaniORCID 0000-0003-4126-3707Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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2022-2022 · peak 1/yr

6 top collaborators · 15 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Anbu Kayalvizhi C.

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1 paper

Genetic & Genomic MedicinemedRxivPreprintSep 13, 2022

Re-analyzing negative exome sequencing data with deep phenotyping identifies pathogenic variants in two patients with suspected Mendelian diseases.

DOI 10.1101/2022.09.13.22279858