Carrier detection and prenatal diagnosis of congenital adrenal hyperplasia must identify 'apparently mild' CYP21A2 alleles which associate neonatal salt-wasting disease

1. Ezquieta, B.
2. Santomé, L.
3. Barrio, R.
4. Barrionuevo, J.L.
5. López-Siguero, J.P.
6. Oliver, A.
7. Ramírez, J.
8. Rodríguez, I.
9. Muñoz-Pacheco, R.