✦ LIBER ✦

P44: Conventional and 1p-specific microarray-based CGH analysis of sporadic and syndrome-related pheochromocytomas

✍ Scribed by Ernst-Jan M. Speel; Marieke Aarts; Hilde Dannenberg; Sandra M. Claessen; Ronald J. de Leeuw; Francien van Nederveen; Albert A. Verhofstad; Winand N. Dinjens; Wan L. Lam; Ronald R. de Krijger

Book ID: 116432918
Publisher: Elsevier Science
Year: 2005
Tongue: English
Weight: 39 KB
Volume: 48
Category: Article
ISSN: 1769-7212
DOI: 10.1016/j.ejmg.2005.10.083

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Microarray-based CGH of sporadic and syn

Microarray-based CGH of sporadic and syndrome-related pheochromocytomas using a 0.1–0.2 Mb bacterial artificial chromosome array spanning chromosome arm 1p

✍ Marieke Aarts; Hilde Dannenberg; Ronald J. deLeeuw; Francien H. van Nederveen; A 📂 Article 📅 2005 🏛 John Wiley and Sons 🌐 English ⚖ 557 KB

## Abstract Pheochromocytomas (PCC) are relatively rare neuroendocrine tumors, mainly of the adrenal medulla. They arise sporadically or occur secondary to inherited cancer syndromes, such as multiple endocrine neoplasia type II (MEN2), von Hippel‐Lindau disease (VHL), or neurofibromatosis type I (