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Endocrine|March 5, 2024
High carrier frequency of CYP21A2 gene mutations in Southern India - underscoring the need for genetic testing in Congenital Adrenal HyperplasiaLavanya Ravichandran, Shriti Paul, Rekha A, et al.Indian Journal of Pediatrics|September 20, 2024
Advocating Targeted Sequential Screening over Whole Exome Sequencing in 21-Hydroxylase DeficiencyLavanya Ravichandran, Shriti Paul, A Rekha, et al.Pageof 1