𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Sequence Variations in the von Hippel–Lindau Tumor Suppressor Gene in Patients with Intracranial Aneurysms

✍ Scribed by Klingler, Jan-Helge; Krüger, Marie T.; Lemke, Johannes R.; Jilg, Cordula; Van Velthoven, Vera; Zentner, Josef; Neumann, Hartmut P.H.; Gläsker, Sven


Book ID
121199637
Publisher
Elsevier Science
Year
2013
Tongue
English
Weight
181 KB
Volume
22
Category
Article
ISSN
1532-8511

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

The von Hippel-Lindau tumor suppressor g
✍ Jasmien Hoebeeck; Jo Vandesompele; Helén Nilsson; Katleen De Preter; Nadine Van 📂 Article 📅 2006 🏛 John Wiley and Sons 🌐 French ⚖ 166 KB

## Abstract Deletions of the short arm of chromosome 3 are often observed in a specific subset of aggressive neuroblastomas (NBs) with loss of distal 11q and without __MYCN__ amplification. The critical deleted region encompasses the locus of the von Hippel‐Lindau gene (__VHL__, 3p25). Constitution