17β-Hydroxysteroid dehydrogenase-3 deficiency: Diagnosis, phenotypic variability, population genetics, and worldwide distribution of ancient and de Novo mutations
BOEHMER, A. L. M, BRINKMANN, A. O, ROUWE, C. W, MENDONCA, B. B, RODRIGUES, C, BODE, H. H, DE RUITER, P. E, DE WAAL, H. A. D.-V, DROP, S. L. S, SANDKUIJL, L. A, HALLEY, D. J. J, NIERMEIJER, M. F, ANDERSSON, S, DE JONG, F. H, KAYSERILI, H, DE VROEDE, M. A, OTTEN, B. J
Published in The journal of clinical endocrinology and metabolism (1999)
Published in The journal of clinical endocrinology and metabolism (1999)
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A limited repertoire of mutations of the luteinizing hormone (LH) receptor gene in familial and sporadic patients with male lh-independent precocious puberty
KREMERT, H, MARTENS, J. W. M, POTAU, N, BUCKLER, J. M. H, JANSEN, M, PARKS, J. S, LATIF, H. A, MOLL, G. W, EPPING, W, SAGGESE, G, MARIMAN, E. C. M, THEMMEN, A. P. N, VAN REEN, M, BRUNNER, H. G, VERHOEF-POST, M, WIT, J. M, OTTEN, B. J, DROP, S. L. S, DE WAAL, H. A. D.-V, POMBO-ARIAS, M, DE LUCA, F
Published in The journal of clinical endocrinology and metabolism (01.03.1999)
Published in The journal of clinical endocrinology and metabolism (01.03.1999)
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Journal Article