𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Germline mutations in the von Hippel–Lindau gene in Italian patients

✍ Scribed by Paola Ciotti; Anna Garuti; Rossella Gulli; Alberto Ballestrero; Emilia Bellone; Paola Mandich


Book ID
116433198
Publisher
Elsevier Science
Year
2009
Tongue
English
Weight
111 KB
Volume
52
Category
Article
ISSN
1769-7212

No coin nor oath required. For personal study only.


📜 SIMILAR VOLUMES


Improved detection of germline mutations
✍ Catherine Stolle; Gladys Glenn; Berton Zbar; Jeffrey S. Humphrey; Peter Choyke; 📂 Article 📅 1998 🏛 John Wiley and Sons 🌐 English ⚖ 201 KB 👁 2 views

Communicated by Victor A. McKusick von Hippel-Lindau disease (VHL) is an inherited neoplastic disorder characterized by the development of tumors in the eyes, brain, spinal cord, inner ear, adrenal gland, pancreas, kidney, and epididymis. The VHL tumor suppressor gene was identified in 1993. Initial

Germline mutation profile of the VHL gen
✍ Sylviane Olschwang; Stéphane Richard; Cécile Boisson; Sophie Giraud; Pierre Laur 📂 Article 📅 1998 🏛 John Wiley and Sons 🌐 English ⚖ 252 KB 👁 2 views

## Communicated by Lap-Chee Tsui Von Hippel-Lindau (VHL) disease is a dominantly inherited disorder predisposing those afflicted to hemangioblastomas of the central nervous system and the retina, renal cell carcinomas, pheochromocytomas, and pancreatic tumors. The disease has been associated with