VHL FAMILY FORUM Volume 18, Number 2

First Page		Document Content
Date: 2012-05-10 21:46:21 Gene expression Tumor suppressor genes Mutation RNA splicing Von Hippel–Lindau tumor suppressor Von Hippel–Lindau disease Hemangioblastoma Pheochromocytoma Genetic code Biology Genetics Medicine		VHL FAMILY FORUM Volume 18, Number 2 Add to Reading List Source URL: vhl.org Download Document from Source Website File Size: 592,88 KB Share Document on Facebook

	MADRID PRESENTATION SUMMARIES Selected lectures and illustrations TABLE OF CONTENTS Basic and clinical research in pheochromocytoma…………………………………………………………………..………… DocID: 11t1Z - View Document
	Protocol to guide the assessment of genetic testing for hereditary mutations in the VHL gene that cause von Hippel-Lindau syndrome May 2011 Table of Contents Table of Tables 3 DocID: VLQ7 - View Document
	Public Summary Document Application No. 1153 – Genetic Testing for Hereditary Mutations in the VHL Gene that Cause von Hippel-Lindau (VHL) syndrome DocID: TRLQ - View Document
	MSAC Draft Evaluation Protocol Scoping Document DocID: ThmD - View Document
	MSAC 54th, Item 4.4, Attachment A Genetic testing for hereditary mutations in the VHL gene that cause von HippelLindau syndrome DocID: SYXa - View Document