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One hundred and seven family members with the rearranged during transfection V804M proto-oncogene mutation presenting with simultaneous medullary and papillary thyroid carcinomas, rare primary hyperparathyroidism, and no pheochromocytomas: Is this a new syndrome–MEN 2C?

✍ Scribed by P.R.K. Bhargav


Book ID
113921526
Publisher
Elsevier Science
Year
2010
Tongue
English
Weight
44 KB
Volume
148
Category
Article
ISSN
0039-6060

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