Year: 2018
Type: Proceeding article
Title: Molecular screening of In2G (c.293-13A/C>G) mutation and detected genotypes among the Macedonian patients with classical form of 21-hydroxylase deficiency
Author: Anastasovska, Violeta
Author: Kochova, Mirjana
Abstract:
Publisher:
Relation: International Journal of Neonatal Screening
Identifier: oai:repository.ukim.mk:20.500.12188/22409
Identifier: http://hdl.handle.net/20.500.12188/22409Identifier: 4
Identifier: 3
