Characterization of 8 Point Mutations in the Cyp21b Gene in Brazilian Patients With Congenital Adrenal Hyperplasia (Cah) Due To 21-Hydroxylase Deficiency 31
| Autor: | Bachega, T AS, Billerbeck, A E C, Madureira, G, Amhold, I J P, Marcondes, J A M, Longui, C A, Medeiros, M A, Bloise, W, Nicolau, W, Mendonça, B B |
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| Zdroj: | Pediatric Research; February 1998, Vol. 43 Issue: 2 p300-300, 1p |
| Databáze: | Supplemental Index |
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