Eunice Marumudi
New Delhi, DL, India
Last Updated: 09/26/2026
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Found 8 publications
Clinical profile and inheritance pattern of CYP21A2 gene mutations in patients with classical congenital adrenal hyperplasia from 10 families.
Journal: Indian journal of endocrinology and metabolism
Published: October 02, 2015
Homozygous p.R246Q Mutation and Impaired Spermatogenesis: Long Term Follow-up of 4 Children from One Family with 5 Alpha Reductase 2 Deficiency.
Journal: Indian journal of pediatrics
Published: April 06, 2015
Gender Issues and Related Social Stigma Affecting Patients with a Disorder of Sex Development in India.
Journal: Archives of sexual behavior
Published: November 21, 2014
5 α-reductase type 2 deficiency - response to dihydrotestosterone gel: correspondence.
Journal: Indian journal of pediatrics
Published: July 15, 2013
Novel nucleotide insertions in two unrelated Indian patients with 5α reductase 2 deficiency leading to premature termination of SRD5A2 enzyme.
Journal: Steroids
Published: May 17, 2013
Diagnosis and management of classical congenital adrenal hyperplasia.
Journal: Steroids
Published: March 31, 2013
Novel mutation of SRD5A2 gene in a patient with 5α-reductase 2 deficiency from India.
Journal: BMJ case reports
Published: November 01, 2012
Molecular genetic analysis of CYP21A2 gene in patients with congenital adrenal hyperplasia.
Journal: Indian journal of endocrinology and metabolism
Published: May 26, 2012
Showing 1-8 of 8
Last Updated: 09/26/2026