Format
Sort by

Send to

Choose Destination

Selected items

Items: 3

1.

High penetrance of pheochromocytoma associated with the novel C634Y/Y791F double germline mutation in the RET protooncogene.

Toledo RA, Wagner SM, Coutinho FL, Lourenço DM Jr, Azevedo JA, Longuini VC, Reis MT, Siqueira SA, Lucon AM, Tavares MR, Fragoso MC, Pereira AA, Dahia PL, Mulligan LM, Toledo SP.

J Clin Endocrinol Metab. 2010 Mar;95(3):1318-27. doi: 10.1210/jc.2009-1355. Epub 2010 Jan 15.

PMID:
20080836
2.

Y791F RET mutation and early onset of medullary thyroid carcinoma in a Brazilian kindred: evaluation of phenotype-modifying effect of germline variants.

Tamanaha R, Camacho CP, Ikejiri ES, Maciel RM, Cerutti JM.

Clin Endocrinol (Oxf). 2007 Nov;67(5):806-8. Epub 2007 Jul 4. No abstract available.

PMID:
17610518
3.

An unusual genotype-phenotype correlation in MEN 2 patients: should screening for RET double germline mutations be performed to avoid misleading diagnosis and treatment?

Cerutti JM, Maciel RM.

Clin Endocrinol (Oxf). 2013 Oct;79(4):591-2. doi: 10.1111/cen.12155. Epub 2013 May 11. No abstract available.

PMID:
23330657

Supplemental Content

Support Center