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Orphanet Journal of Rare Diseases|April 28, 2022
Genetic insight into Birt-Hogg-Dubé syndrome in Indian patients reveals novel mutations at FLCNAnindita Ray, Esita Chattopadhyay, Richa Singh, et al.
Expert Opinion on Biological Therapy|September 1, 2021
Analytical similarity assessment of MYL-1402O to reference BevacizumabParag Goyal, Bhavesh Vats, Malini Subbarao, et al.
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