Low Frequency of CYP21B Deletions in Brazilian Patients with Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency

Publisher: Karger

E-ISSN: 1423-0062|49|1|9-14

ISSN: 0001-5652

Source: Human Heredity, Vol.49, Iss.1, 1999-01, pp. : 9-14

Disclaimer: Any content in publications that violate the sovereignty, the constitution or regulations of the PRC is not accepted or approved by CNPIEC.

Previous Menu Next

Abstract

Related content