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An Uncommon Phenotype with Familial Central Hypogonadism Ca..:
Reynaud, Rachel
;
Barlier, Anne
;
Vallette-Kasic, Sophie
...
The Journal of Clinical Endocrinology & Metabolism. 90 (2005) 8 - p. 4880-4887 , 2005
Link:
https://doi.org/10.1210/jc.2005-0119
RT Journal T1 <Title>An Uncommon Phenotype with Familial Central Hypogonadism Caused by a Novel PROP1 Gene Mutant Truncated in the Transactivation Domain</Title> UL https://suche.suub.uni-bremen.de/peid=cr-10.1210_jc.2005-0119&Exemplar=1&LAN=DE A1 Reynaud, Rachel A1 Barlier, Anne A1 Vallette-Kasic, Sophie A1 Saveanu, Alexandru A1 Guillet, Marie-Pierre A1 Simonin, Gilbert A1 Enjalbert, Alain A1 Valensi, Paul A1 Brue, Thierry PB The Endocrine Society YR 2005 SN 0021-972X SN 1945-7197 JF The Journal of Clinical Endocrinology & Metabolism VO 90 IS 8 SP 4880 OP 4887 LK http://dx.doi.org/https://doi.org/10.1210/jc.2005-0119 DO https://doi.org/10.1210/jc.2005-0119 SF ELIB - SuUB Bremen
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