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POINT MUTATIONS IN ITALIAN PATIENTS WITH CLASSIC, NONCLASSIC, AND CRYPTIC FORMS OF STEROID 21-HYDROXYLASE DEFICIENCY
Authors: CARRERA P BORDONE L AZZANI T BRUNELLI V GARANCINI MP CHIUMELLO G FERRARI M
Citation: P. Carrera et al., POINT MUTATIONS IN ITALIAN PATIENTS WITH CLASSIC, NONCLASSIC, AND CRYPTIC FORMS OF STEROID 21-HYDROXYLASE DEFICIENCY, Human genetics, 98(6), 1996, pp. 662-665
CAG TRIPLET ANALYSIS IN FAMILIES WITH ANDROGEN INSENSITIVITY SYNDROMEBY CAPILLARY ELECTROPHORESIS IN POLYMER NETWORKS
Authors: GELFI C RIGHETTI PG LEONCINI F BRUNELLI V CARRERA P FERRARI M
Citation: C. Gelfi et al., CAG TRIPLET ANALYSIS IN FAMILIES WITH ANDROGEN INSENSITIVITY SYNDROMEBY CAPILLARY ELECTROPHORESIS IN POLYMER NETWORKS, Journal of chromatography, 706(1-2), 1995, pp. 463-468
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