Found: 4
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Absence of Mutation in the Follicle-Stimulating Hormone Receptor Gene in Severe Primary Hypothyroidism Associated with Gonadal Hyperstimulation.
- Published in:
- Journal of Pediatric Endocrinology & Metabolism, 2007, v. 20, n. 8, p. 923, doi. 10.1515/jpem.2007.20.8.923
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- Publication type:
- Article
Ethmoid glomangioma and oncogenic osteomalacia: a case report.
- Published in:
- 2021
- By:
- Publication type:
- journal article
A single somatic activating Asp578His mutation of the luteinizing hormone receptor causes Leydig cell tumour in boys with gonadotropin-independent precocious puberty.
- Published in:
- 2006
- By:
- Publication type:
- Letter
A signal peptide mutation of the arginine vasopressin gene in monozygotic twins.
- Published in:
- Clinical Endocrinology, 2003, v. 58, n. 1, p. 108, doi. 10.1046/j.1365-2265.2003.01667.x
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- Publication type:
- Article