共 28 条
- [2] A MISSENSE MUTATION IN THE 2ND TRANSMEMBRANE SEGMENT OF THE LUTEINIZING-HORMONE RECEPTOR CAUSES FAMILIAL MALE-LIMITED PRECOCIOUS PUBERTY JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1995, 80 (11): : 3168 - 3172
- [7] A NEW CONSTITUTIVELY ACTIVATING POINT MUTATION IN THE LUTEINIZING-HORMONE CHORIOGONADOTROPIN RECEPTOR GENE IN CASES OF MALE-LIMITED PRECOCIOUS PUBERTY JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1995, 80 (04): : 1162 - 1168
- [8] A SPORADIC CASE OF MALE-LIMITED PRECOCIOUS PUBERTY HAS THE SAME CONSTITUTIVELY ACTIVATING POINT MUTATION IN LUTEINIZING-HORMONE CHORIOGONADOTROPIN RECEPTOR GENE AS FAMILIAL CASES JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1994, 79 (06): : 1818 - 1823