Mehta, Sneha P.

Comprehensive genetic analysis of 182 unrelated families with congenital adrenal hyperplasia due to 21-hydroxylase deficiency

Finkielstain, G. P., Chen, W., Mehta, S. P., Fujimura, F. K., Hanna, R. M., Van Ryzin, C., McDonnell, N. B., & Merke, D. P. (2011) · The Journal of Clinical Endocrinology & Metabolism

Sexual Differentiation and DisordersAdrenal Hormones and Disorders

Cited by 192

Phenotypic profiling of parents with cryptic nonclassic congenital adrenal hyperplasia: findings in 145 unrelated families

Nandagopal, R., Sinaii, N., Avila, N. A., Van Ryzin, C., Chen, W., Finkielstain, G. P., Mehta, S. P., McDonnell, N. B., & Merke, D. P. (2011) · European Journal of Endocrinology

Sexual Differentiation and DisordersAdrenal Hormones and Disorders

Cited by 81

Adrenomedullary Function in Patients with Nonclassic Congenital Adrenal Hyperplasia

Verma, S., Green-Golan, L., VanRyzin, C., Drinkard, B., Mehta, S. P., Weise, M., Eisenhofer, G., & Merke, D. P. (2010) · Hormone and Metabolic Research

Sexual Differentiation and DisordersAdrenal Hormones and Disorders

Cited by 24