Low frequency of CYP2B deletions in Brazilian patients with congenital adrenal hyperplasia due to 21-hydroxylas deficiency

Bachega, T A ; Billerbeck, A E ; Madureira, G ; Arnhold, I J ; Medeiros, M A ; Marcondes, J A ; Longui, C A ; Nicolau, W ; Bloise, W ; Mendonca, B B

Human heredity, 1999-01, Vol.49 (1), p.9-14 [Periódico revisado por pares]

Switzerland

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