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

Autor:	Bachega, Tânia A.S.S., Billerbeck, Ana Elisa C., Madureira, Guiomar, Arnhold, Ivo J.P., Medeiros, Maria A., Marcondes, José A.M., Longui, Carlos A., Nicolau, Willian, Bloise, Walter, Mendonca, Berenice B.
Zdroj:	Human Heredity, 1999 Jan 01. 49(1), 9-14.
Databáze:	JSTOR Journals
Externí odkaz:	https://www.jstor.org/stable/48506697 Zobrazit plný text záznamu