Rationalization of genetic testing in patients with apparently sporadic pheochromocytoma/paraganglioma

Hormone and Metabolic Research

Volumn 41, Issue 9, 2009, Pages 672-675

  Cascon A ^a   Lopez Jimenez E ^a   Landa, I ^a   Leskela S ^a   Leandro Garcia L J ^a   Maliszewska, A ^a   Leton R ^a   Vega, L De La ^a   Garcia Barcina M J ^b   Sanabria, C ^c   Alvarez Escola C ^d   Rodriguez Antona C ^a   Robledo, M ^a  

^a Centro Nacional de Investigaciones Oncológicas   (Spain)

^b HOSPITAL DE BASURTO   (Spain)

^c HOSPITAL CLÍNICO SAN CARLOS   (Spain)

^d HOSPITAL UNIVERSITARIO LA PAZ   (Spain)

Author keywords

Apparently sporadic; Paraganglioma; Pheochromocytoma; SDHB

Indexed keywords

VON HIPPEL LINDAU PROTEIN;

ADOLESCENT; ADULT; AGED; ARTICLE; CHILD; CONTROLLED STUDY; FRAMESHIFT MUTATION; GENE DELETION; GENETIC SCREENING; GENETIC SUSCEPTIBILITY; GERM LINE; GROUPS BY AGE; HEAD AND NECK TUMOR; HUMAN; MAJOR CLINICAL STUDY; MISSENSE MUTATION; ONCOGENE RET; PARAGANGLIOMA; PHEOCHROMOCYTOMA; PRIORITY JOURNAL; SCHOOL CHILD; SDHB GENE; SDHC GENE; SDHD GENE; SPLICING DEFECT; TUMOR SUPPRESSOR GENE;

ADOLESCENT; ADRENAL GLAND NEOPLASMS; ADULT; AGED; FEMALE; GENETIC SCREENING; GERM-LINE MUTATION; HUMANS; MALE; MIDDLE AGED; PARAGANGLIOMA; PHEOCHROMOCYTOMA; PROTO-ONCOGENE PROTEINS C-RET; SUCCINATE DEHYDROGENASE; VON HIPPEL-LINDAU TUMOR SUPPRESSOR PROTEIN; YOUNG ADULT;

EID: 70350211961     PISSN: 00185043     EISSN: 14394286     Source Type: Journal    
DOI: 10.1055/s-0029-1202814     Document Type: Article

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