One hundred and seven member family 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 Alexander L. Shifrin; Angela M. Fay; Cristina Z. Xenachis; Jerome J. Vernick

• Book ID: 113921557
• Publisher: Elsevier Science
• Year: 2010
• Tongue: English
• Weight: 39 KB
• Volume: 148
• Category: Article
• ISSN: 0039-6060
• DOI: 10.1016/j.surg.2010.06.006