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ABSENCE OF MOLECULAR DEFECT IN THE TYPE-II 3-BETA-HYDROXYSTEROID DEHYDROGENASE (3-BETA-HSD) GENE IN PREMATURE PUBARCHE CHILDREN AND HIRSUTEFEMALE-PATIENTS WITH MODERATELY DECREASED ADRENAL 3-BETA-HSD ACTIVITY
Authors: CHANG YT ZHANG L ALKADDOUR HS MASON JI LIN KM YANG XJ GARIBALDI LR BOURDONY CJ DOLAN LM DONALDSON DL PANG SY
Citation: Yt. Chang et al., ABSENCE OF MOLECULAR DEFECT IN THE TYPE-II 3-BETA-HYDROXYSTEROID DEHYDROGENASE (3-BETA-HSD) GENE IN PREMATURE PUBARCHE CHILDREN AND HIRSUTEFEMALE-PATIENTS WITH MODERATELY DECREASED ADRENAL 3-BETA-HSD ACTIVITY, Pediatric research, 37(6), 1995, pp. 820-824
A NEW HETEROZYGOUS MUTATION IN TYPE-II 3-BETA-HYDROXYSTEROID DEHYDROGENASE (3-BETA-HSD) GENE CAUSING SALT-WASTING 3-DELTA-HSD DEFICIENCY CONGENITAL ADRENAL-HYPERPLASIA (CAH)
Authors: ZHANG L ALKADDOUR HS CHANG YT YANG XJ PANG SY
Citation: L. Zhang et al., A NEW HETEROZYGOUS MUTATION IN TYPE-II 3-BETA-HYDROXYSTEROID DEHYDROGENASE (3-BETA-HSD) GENE CAUSING SALT-WASTING 3-DELTA-HSD DEFICIENCY CONGENITAL ADRENAL-HYPERPLASIA (CAH), Pediatric research, 37(4), 1995, pp. 102-102
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