SDHB mutation analysis in familial and sporadic phaeochromocytoma identifies a novel mutation

被引：14

作者：

Cascon, A. ^{[1
]}

Cebrian, A. ^{[1
]}

Ruiz-Llorente, S. ^{[1
]}

Telleria, D. ^{[1
]}

Benitez, J. ^{[1
]}

Robledo, M. ^{[1
]}

机构：

[1] Spanish Natl Canc Ctr CNIO, Dept Human Genet, Madrid, Spain

来源：

JOURNAL OF MEDICAL GENETICS | 2002年 / 39卷 / 10期

关键词：

D O I：

10.1136/jmg.39.10.e64

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

[No abstract available]

引用

页数：3

共 14 条

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[J]. CLINICAL ENDOCRINOLOGY, 2002, 56 (01) : 113 - 117
[8] Gimm O, 2000, CANCER RES, V60, P6822
[9] Absence of SDHD mutations in primary nasopharyngeal carcinomas
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[J]. INTERNATIONAL JOURNAL OF CANCER, 2002, 97 (06) : 875 - 877
[10] Phenotypic expression in von Hippel-Lindau disease: Correlations with germline VHL gene mutations
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[J]. JOURNAL OF MEDICAL GENETICS, 1996, 33 (04) : 328 - 332

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