Erlic, Z.

paraganglioma tumor mutation vhl gene vhl disease disease patient analysis pheochromocytoma syndrome hippel-lindau germline allele tumor cells von hippel-lindau disease case 1 chromosome cell carcinomas marker sequencing endocrinol metab krijger rr mutation analysis study addition family result cancer harbor vhl deletions vhl type 2. carcinoma wildtype vhl allele vhl patients inactivation hemangioblastoma tumor dna sdhd genes biallelic inactivation chromosome 3 p vhl syndrome lenders jw chromosome 11 wild-type vhl allele harbor missense mutations loh analysis vhl germline mutation endolymphatic sac tumors vhl type 1 neck paragangliomas tumor suppressor gene carotid case 2 krijger 64pro department genomic sample dinjen november genet wild-type missense p.arg truncating mutations chromatogram p.tyr fibrovascular stroma von hippel-lindau linehan wm deletion genomic hybridization microsatellite loci dinjens wn tissue plouin pf region wild-type allele catecholamines microsatellite