158 TRANSDERMAL DIHYDROTESTOSTERONE TREATMENT FOR THREE PATIENTS WITH STEROID 5α REDUCTASE-2 DEFICIENCY

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29 TURNER SYNDROME AND XP DELETIONS : CLINICAL AND MOLECULAR STUDIES IN 47 PATIENTS
68 Four cases of Kallmann syndrome with FGFR1 mutations
33 LONG-TERM PROGNOSIS IN ADULT MALES WITH CLASSICAL 21-HYDROXYLASE DEFICIENCY
97 A FEMALE INFANT WITH 21-HYDROXYLASE DEFICIENCY WHO HAD THE VAGINAL ENLARGEMENT
94 MEASUREMENTS OF SERUM 17-HYDROXYPROGESTERONE IN NEWBORN INFANTS BY STABLE ISOTOPE DILUTION / GAS CHROMATOGRAPHY-MASS SPECTROMETRY
111 EFFECTS OF LONG-TERM TESTOSTERONE THERAPY ON BONE MINERAL DENSITY IN MALE WITH HYPOGONADOTROPIC HYPOGONADISM
36 CONGENITAL ADRENAL HYPOPLASIA AND MENTAL RETARDATION : IMPORTNACE OF THE IL1RAPL GENE ANALYSIS
30 SHOX NULLIZYGOSITY AND HAPLOINSUFFICIENCY IN A JAPANESE FAMILY : IMPLICATION FOR THE DEVELOPMENT OF TURNER SKELETAL FEATURES.
66 URINE 5β/5α-REDUCED STEROID RATIO : INFLUENCE OF MUTAIONS AND POLYMORPHISM OF THE STEROID 5α REDUCTASE-2 GENE
158 TRANSDERMAL DIHYDROTESTOSTERONE TREATMENT FOR THREE PATIENTS WITH STEROID 5α REDUCTASE-2 DEFICIENCY

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