VHL FAMILY FORUM Volume 14, Number 1

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Date: 2012-05-11 07:26:23 Kidney cancer Tumor suppressor genes Rare diseases Von Hippel–Lindau tumor suppressor Von Hippel–Lindau disease Pheochromocytoma Hemangioblastoma Renal cell carcinoma Prostate cancer Medicine Oncology Health		VHL FAMILY FORUM Volume 14, Number 1 Add to Reading List Source URL: vhl.org Download Document from Source Website File Size: 385,71 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