Petri, B.J.

mutation phaeochromocytoma patient paraganglioma tumours syndrome tumour pheochromocytoma testing germline immunohistochemistry 12 months sdhb immunohistochemistry surgery surgery society ltd month disease screening adrenalectomy cancer result germline mutations study phaeochromocytoma –paraganglioma syndrome british journal john wiley series family analysis succinate tissue follow-up fferent department –lindau laparoscopic treatment hippel medullary thyroid carcinoma www.bjs.co.uk british journal endocrinol van nederveen fh protein sdhd mutation speci ficity absence sdhb immunostaining mitochondrial tumour cells type 2 –paraganglioma sdhd mutations expression antibody wiley subunit chromosome resection dehydrogenase staining family members linehan wm sdh mutation men 2 van eijck metab 1381–1392 succinate dehydrogenase subunit sdh enzyme activity society krijger www.bjs.co.uk ret proto-oncogene immunohistochemical entity sample netherland university copyright