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Results: 1-10 |
Results: 10
INACTIVATION OF THE LUTEINIZING HORMONE CHORIONIC GONADOTROPIN RECEPTOR BY AN INSERTIONAL MUTATION IN LEYDIG-CELL HYPOPLASIA/
Authors: WU SM HALLERMEIER KM LAUE L BRAIN C BERRY AC GRANT DB GRIFFIN JE WILSON JD CUTLER GB CHAN WY
Citation: Sm. Wu et al., INACTIVATION OF THE LUTEINIZING HORMONE CHORIONIC GONADOTROPIN RECEPTOR BY AN INSERTIONAL MUTATION IN LEYDIG-CELL HYPOPLASIA/, Molecular endocrinology, 12(11), 1998, pp. 1651-1660
LASER-ASSISTED ENDOSCOPIC FOREHEAD LIFT
Authors: GRIFFIN JE FREY BS MAX DP EPKER BN
Citation: Je. Griffin et al., LASER-ASSISTED ENDOSCOPIC FOREHEAD LIFT, Journal of oral and maxillofacial surgery, 56(9), 1998, pp. 1040-1048
OBJECTIVE EVALUATION OF THE EYELIDS AND EYEBROWS AFTER BLEPHAROPLASTY
Authors: STARCK WJ GRIFFIN JE EPKER BN
Citation: Wj. Starck et al., OBJECTIVE EVALUATION OF THE EYELIDS AND EYEBROWS AFTER BLEPHAROPLASTY, Journal of oral and maxillofacial surgery, 54(3), 1996, pp. 297-302
MOLECULAR-GENETICS AND PATHOPHYSIOLOGY OF 17-BETA-HYDROXYSTEROID DEHYDROGENASE-3 DEFICIENCY
Authors: ANDERSSON S GEISSLER WM WU L DAVIS DL GRUMBACH MM NEW MJ SCHWARZ HP BLETHEN SL MENDONCA BB BLOISE W WITCHEL SF CUTLER GB GRIFFIN JE WILSON JD RUSSELL DW
Citation: S. Andersson et al., MOLECULAR-GENETICS AND PATHOPHYSIOLOGY OF 17-BETA-HYDROXYSTEROID DEHYDROGENASE-3 DEFICIENCY, The Journal of clinical endocrinology and metabolism, 81(1), 1996, pp. 130-136
A NONSENSE MUTATION OF THE HUMAN LUTEINIZING-HORMONE RECEPTOR GENE INLEYDIG-CELL HYPOPLASIA
Authors: LAUE L WU SM KUDO M HSUEH AJW CUTLER GB GRIFFIN JE WILSON JD BRAIN C BERRY AC GRANT DB CHAN WY
Citation: L. Laue et al., A NONSENSE MUTATION OF THE HUMAN LUTEINIZING-HORMONE RECEPTOR GENE INLEYDIG-CELL HYPOPLASIA, Human molecular genetics, 4(8), 1995, pp. 1429-1433
MUTATIONS OF THE ANDROGEN RECEPTOR CODING SEQUENCE ARE INFREQUENT IN PATIENTS WITH ISOLATED HYPOSPADIAS
Authors: ALLERA A HERBST MA GRIFFIN JE WILSON JD SCHWEIKERT HU MCPHAUL MJ
Citation: A. Allera et al., MUTATIONS OF THE ANDROGEN RECEPTOR CODING SEQUENCE ARE INFREQUENT IN PATIENTS WITH ISOLATED HYPOSPADIAS, The Journal of clinical endocrinology and metabolism, 80(9), 1995, pp. 2697-2699
AMINO-ACID SUBSTITUTIONS IN THE HORMONE-BINDING DOMAIN OF THE HUMAN ANDROGEN RECEPTOR ALTER THE STABILITY OF THE HORMONE-RECEPTOR COMPLEX
Authors: MARCELLI M ZOPPI S WILSON CM GRIFFIN JE MCPHAUL MJ
Citation: M. Marcelli et al., AMINO-ACID SUBSTITUTIONS IN THE HORMONE-BINDING DOMAIN OF THE HUMAN ANDROGEN RECEPTOR ALTER THE STABILITY OF THE HORMONE-RECEPTOR COMPLEX, The Journal of clinical investigation, 94(4), 1994, pp. 1642-1650
LEYDIG-CELL NEOPLASIA IN A PATIENT WITH REIFENSTEIN SYNDROME
Authors: JOCKENHOVEL F RUTGERS JKL MASON JS GRIFFIN JE SWERDLOFF RS
Citation: F. Jockenhovel et al., LEYDIG-CELL NEOPLASIA IN A PATIENT WITH REIFENSTEIN SYNDROME, Experimental and clinical endocrinology, 101(6), 1993, pp. 365-370
STEROID 5-ALPHA-REDUCTASE-2 DEFICIENCY
Authors: WILSON JD GRIFFIN JE RUSSELL DW
Citation: Jd. Wilson et al., STEROID 5-ALPHA-REDUCTASE-2 DEFICIENCY, Endocrine reviews, 14(5), 1993, pp. 577-593
GENETIC-BASIS OF ENDOCRINE DISEASE .4. THE SPECTRUM OF MUTATIONS IN THE ANDROGEN RECEPTOR GENE THAT CAUSES ANDROGEN RESISTANCE
Authors: MCPHAUL MJ MARCELLI M ZOPPI S GRIFFIN JE WILSON JD
Citation: Mj. Mcphaul et al., GENETIC-BASIS OF ENDOCRINE DISEASE .4. THE SPECTRUM OF MUTATIONS IN THE ANDROGEN RECEPTOR GENE THAT CAUSES ANDROGEN RESISTANCE, The Journal of clinical endocrinology and metabolism, 76(1), 1993, pp. 17-23
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