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Idiopathic gonadotrophin deficiency: genetic questions addressed through phenotypic characterization

Quinton, R; Duke, VM; Robertson, A; Kirk, JMW; Matfin, G; de Zoysa, PA; Azcona, C; ... Bouloux, PMG; + view all (2001) Idiopathic gonadotrophin deficiency: genetic questions addressed through phenotypic characterization. CLINICAL ENDOCRINOLOGY , 55 (2) pp. 163-174. 10.1046/j.1365-2265.2001.01277.x.

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Type: Article
Title: Idiopathic gonadotrophin deficiency: genetic questions addressed through phenotypic characterization
Location: NEW ORLEANS, LA
DOI: 10.1046/j.1365-2265.2001.01277.x
Keywords: Science & Technology, Life Sciences & Biomedicine, Endocrinology & Metabolism, LINKED KALLMANN-SYNDROME, ISOLATED HYPOGONADOTROPIC HYPOGONADISM, ADRENAL HYPOPLASIA CONGENITA, HORMONE-RELEASING HORMONE, UNILATERAL RENAL APLASIA, MIRROR MOVEMENTS, DEVELOPMENTAL ANOMALIES, CANDIDATE GENE, MUTATIONS, RECEPTOR
UCL classification: UCL > Provost and Vice Provost Offices
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Medical Sciences
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Medical Sciences > Div of Medicine
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Medical Sciences > Div of Medicine > Metabolism and Experi Therapeutics
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Pop Health Sciences > Inst for Women's Health
URI: http://discovery.ucl.ac.uk/id/eprint/27217
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