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American Journal of Otology
Volumn 20, Issue 5, 1999, Pages 639-643
Familial paragangliomas: The emerging impact of molecular genetics on evaluation and management
Author keywords

Familial paragangliomas; Gene mapping; Microsatellite markers; Presymptomatic screening
Indexed keywords

ADULT; AMNION FLUID ANALYSIS; ARTICLE; AUTOSOMAL DOMINANT DISORDER; CARCINOGENESIS; CHROMOSOME 11Q; CHROMOSOME MAP; CLINICAL ARTICLE; FEMALE; GENETIC SCREENING; GENOME IMPRINTING; HAPLOTYPE; HEARING LOSS; HUMAN; MOLECULAR GENETICS; NECK TUMOR; PARAGANGLIOMA; PRIORITY JOURNAL;
EID: 0033490101     PISSN: 01929763     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (44)
References (10)
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    • A gene subject to genomic imprinting and responsible for hereditary paragangliomas maps to chromosome 11q23-qter
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  • 5
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    • Devilee P, van Schothorst EM, Bardoel AF, et al. Allelotype of head and neck paragangliomas: allelic imbalance is confined to the long arm of chromosome 11, the site of the predisposing locus PGL. Genes Chromosomes Cancer 1994;11:71-8.
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    • Devilee, P.1    Van Schothorst, E.M.2    Bardoel, A.F.3
  • 6
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    • Fine mapping of a putatively imprinted gene for familial non-chromaffin paragangliomas to chromosome 11q13.1:Evidence for genetic heterogeneity
    • Mariman EC, van Beersum SE, Cremers CW, et al. Fine mapping of a putatively imprinted gene for familial non-chromaffin paragangliomas to chromosome 11q13.1:evidence for genetic heterogeneity. Hum Genet 1995;95:56-62.
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  • 8
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.