相关参考文献
注意:仅列出部分参考文献,下载原文获取全部文献信息。What Have We Learned from Molecular Biology of Paragangliomas and Pheochromocytomas?
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Somatic and germline mutations in the pathogenesis of pituitary adenomas
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Low penetrance of paraganglioma and pheochromocytoma in an extended kindred with a germline SDHB exon 3 deletion
J. A. Rijken et al.
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A SDHC Founder Mutation Causes Paragangliomas (PGLs) in the French Canadians: New Insights on the SDHC-Related PGL
Isabelle Bourdeau et al.
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McCune-Albright Syndrome: A Detailed Pathological and Genetic Analysis of Disease Effects in an Adult Patient
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A founder SDHB mutation in Portuguese paraganglioma patients
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Genetic analysis in young patients with sporadic pituitary macroadenomas: besides AIP don't forget MEN1 genetic analysis
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High prevalence of founder mutations of the succinate dehydrogenase genes in the Netherlands
E. F. Hensen et al.
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Familial Carotid Body Tumors in Patients withSDHDMutations: A Case Series
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The Endemic Paraganglioma Syndrome Type 1: Origin, Spread, and Clinical Expression
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Mutations in SDHD are the major determinants of the clinical characteristics of Dutch head and neck paraganglioma patients
E. F. Hensen et al.
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Strong Maternal Khoisan Contribution to the South African Coloured Population: A Case of Gender-Biased Admixture
Lluis Quintana-Murci et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2010)
The first Dutch SDHB founder deletion in paraganglioma-pheochromocytoma patients
Jean-Pierre Bayley et al.
BMC MEDICAL GENETICS (2009)
Mediastinal paragangliomas: association with mutations in the succinate dehydrogenase genes and aggressive behavior
Hans K. Ghayee et al.
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High frequency of germline succinate dehydrogenase mutations in sporadic cervical paragangliomas in Northern Spain:: Mitochondrial succinate dehydrogenase structure-function relationships and clinical-pathological correlations
Jorge Lima et al.
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Frederieke M. Brouwers et al.
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM (2006)
Clinical presentation and penetrance of pheochromocytoma/paraganglioma syndromes
DE Benn et al.
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Mutation analysis of SDHB and SDHC: novel germline mutations in sporadic head and neck paraganglioma and familial paraganglioma and/or pheochromocytoma
JP Bayley et al.
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Founder mutations among the Dutch
MPA Zeegers et al.
EUROPEAN JOURNAL OF HUMAN GENETICS (2004)
Nearly all hereditary paragangliomas in the Netherlands are caused by two founder mutations in the SDHD gene
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