Prenatal diagnosis of steroid 21-hydroxylase deficiency by allele-specific amplification.
Autor: | Theodoropoulou, Marily, Barta, Csaba, Szoke, Melinda, Guttman, András, Staub, Maria, Niederland, Tamás, Sólyom, János, Fekete, György, Sasvari-Szekely, Maria, Theodoropoulou, M, Barta, C, Szoke, M, Guttman, A, Staub, M, Niederland, T, Sólyom, J, Fekete, G, Sasvari-Szekely, M |
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Zdroj: | Fetal Diagnosis & Therapy; 2001, Vol. 16 Issue 4, p237-240, 4p |
Databáze: | Complementary Index |
Externí odkaz: |