Molecular pathogenesis in sporadic head and neck paraganglioma

Laryngoscope

Volumn 110, Issue 8, 2000, Pages 1346-1348

  Bikhazi, Paul H ^a,b   Messina, Louis ^a   Mhatre, Anand N ^a   Goldstein, Jayne A ^a   Lalwani, Anil K ^a,b  

^a UNIVERSITY OF CALIFORNIA   (United States)

^b UNIVERSITY OF CALIFORNIA   (United States)

Author keywords

Allelic imbalance; Loss of heterozygosity; Microsatellite markers; Sporadic paragangliomas

Indexed keywords

ADULT; AGED; ARTICLE; CHROMOSOME 11Q; CHROMOSOME DELETION; CLINICAL ARTICLE; DISEASE ASSOCIATION; FAMILIAL DISEASE; HUMAN; MICROSATELLITE INSTABILITY; PARAGANGLIOMA; PATHOGENESIS; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL;

EID: 0033869351     PISSN: 0023852X     EISSN: None     Source Type: Journal    
DOI: 10.1097/00005537-200008000-00023     Document Type: Article

References (9)

1. A gene subject to genomic imprinting and responsible for hereditary paragangliomas maps to chromosome 11q23-qter
2. Allelotype of head and neck paragangliomas allelic imbalance is confined to the long arm of chromosome 11, the site of the a predisposing locus PGL
3. Fine mapping of a putatively imprinted gene for familial non-chromaffin paragangliomas to chromosome 11q13.1: Evidence for genetic heterogeneity
4. A high resolution STS, EST, and gene-based map of the hereditary paraganglioma region of chromosome 11q23
5. Fine mapping of an imprinted gene for familial non-chromaffin paragangliomas, on chromosome 11q23
6. Loss of heterozygosity on the short arm of chromosome 1 and 3 in sporadic pheochromocytoma and extra-adrenal paraganglioma
7. Loss of heterozygosity in 11q13-14 regions in gastric neuroendocrine tumors not associated with multiple endocrine neoplasia type 1 syndrome
8. Metastatic retroperitoneal paraganglioma in a 16-year-old girl. Case report, molecular pathological and cytogenetic findings
9. Familial paragangliomas: The emerging impact of molecular genetics on evaluation and management