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Volumn 51, Issue 9, 2007, Pages 1463-1467

Molecular analysis of the Von Hippel-Lindau (VHL) gene in a family with non-syndromic pheochromocytoma: The importance of genetic testing

Author keywords

Genetic testing; Mutation; Pheochromocytoma; Von Hippel Lindau disease

Indexed keywords


EID: 38849189979     PISSN: 00042730     EISSN: 16779487     Source Type: Journal    
DOI: 10.1590/S0004-27302007000900008     Document Type: Article
Times cited : (7)

References (14)
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  • 4
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  • 5
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    • Phenotypic expression in von Hippel-Lindau disease: Correlations with germline VHL gene mutations
    • Maher ER, Webster AR, Richards FM, Green JS, Crossey PA, Payne SJ, et al. Phenotypic expression in von Hippel-Lindau disease: correlations with germline VHL gene mutations. J Med Genet 1996;33(4):328-32.
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    • Maher, E.R.1    Webster, A.R.2    Richards, F.M.3    Green, J.S.4    Crossey, P.A.5    Payne, S.J.6
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  • 7
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    • VHL2C phenotype in a German von Hippel-Lindau family with concurrent VHL germline mutations P81S and L188V
    • Weirich G, Klein B, Wöhl T, Engelhardt D, Brauch H. VHL2C phenotype in a German von Hippel-Lindau family with concurrent VHL germline mutations P81S and L188V. J Clin Endocrinol Metab 2002;87(11):5241-6.
    • (2002) J Clin Endocrinol Metab , vol.87 , Issue.11 , pp. 5241-5246
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  • 8
    • 19944425515 scopus 로고    scopus 로고
    • Pheochromocytoma-associated syndromes: Genes, proteins and functions of RET, VHL and SDHx
    • Gimm O. Pheochromocytoma-associated syndromes: genes, proteins and functions of RET, VHL and SDHx. Fam Cancer 2005;4(1):17-23.
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  • 9
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  • 10
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    • Genotype-phenotype correlations in families with deletions in the von Hippel-Lindau (VHL) gene
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    • Clinical utility of noncontrast computed tomography attenuation value (Hounsfield units) to differentiate adrenal adenomas/hyperplasias from nonadenomas: Cleveland Clinic experience
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.