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Endocrinology

  
 
Results: Displaying 10 of 252 on page 14 of 26
Name
Title
Area
Document
Colleges
Year
Mutation screening in the VHL, SDHB and SDHD genes in patients with sporadic pheochromocytoma...
Inactivating mutations in the MKRN3 gene are cause of familial central precocious...
Search for mutations on FGF9 and FGFR2 genes in patients with 46,XY disorders of...
Study of mRNA expression of the receptors for vasopressin (AVPR1B), corticotropin...
Secretory profile of growth hormone and ghrelin before and after bariatric surge...
Growth hormone (GH) treatment of children with GH deficiency: importance of IGF-I...
Study of Tbx19 and Crhr1 genes in Poodle dogs with ACTH-dependent hypercortisoli...
Analysis of the allelic variants of the armadillo repeat containing 5 (ARMC5) gene...
Standardization of the PNA and real time techniques for the detection of activating...
Results: Displaying 10 of 252 on page 14 of 26
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