The penetrance of paraganglioma and pheochromocytoma in SDHB germline mutation carriers-Reference-Cited by-同舟云学术

The penetrance of paraganglioma and pheochromocytoma in SDHB germline mutation carriers

Published:2017-09-06 Issue:1 Volume:93 Page:60-66
ISSN:0009-9163
Container-title:Clinical Genetics
language:en
Short-container-title:Clin Genet

Author:

Rijken J.A.¹^ORCID,Niemeijer N.D.²,Jonker M.A.³⁴,Eijkelenkamp K.⁵,Jansen J.C.⁶,van Berkel A.⁷,Timmers H.J.L.M⁷,Kunst H.P.M.⁸,Bisschop P.H.L.T.⁹,Kerstens M.N.⁵,Dreijerink K.M.A.¹⁰,van Dooren M.F.¹¹,van der Horst-Schrivers A.N.A.⁵,Hes F.J.¹²^ORCID,Leemans C.R.¹,Corssmit E.P.M.²,Hensen E.F.¹¹³

Affiliation:

1. Department of Otorhinolaryngology - Head and Neck Surgery; VU University Medical Center; Amsterdam the Netherlands

2. Department of Endocrinology and Metabolic Diseases; Leiden University Medical Center; Leiden the Netherlands

3. Department of Epidemiology and Biostatistics; VU University Medical Center; Amsterdam the Netherlands

4. Department for Health Evidence; Radboud University medical center; Nijmegen the Netherlands

5. Department of Endocrinology, University of Groningen; University Medical Center Groningen; Groningen the Netherlands

6. Department of Otorhinolaryngology; Leiden University Medical Center; Leiden the Netherlands

7. Division of Endocrinology, Department of Internal Medicine; Radboud University Medical Center; Nijmegen the Netherlands

8. Department of Otorhinolaryngology - Head and Neck Surgery, Radboud Institute of Health Sciences; Radboud University Medical Center; Nijmegen the Netherlands

9. Department of Endocrinology and Metabolism, Academic Medical Center; University of Amsterdam; Amsterdam the Netherlands

10. Department of Endocrinology; University Medical Centre Utrecht; Utrecht the Netherlands

11. Department of Clinical Genetics, Erasmus MC; University Medical Center Rotterdam; Rotterdam the Netherlands

12. Department of Clinical Genetics; Leiden University Medical Center; Leiden the Netherlands

13. Department of Otorhinolaryngology - Head and Neck Surgery; Leiden University Medical Center; Leiden the Netherlands

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/cge.13055/fullpdf

Reference26 articles.

1. Whole-exome sequencing identifies MDH2 as a new familial paraganglioma gene;Cascon;J Natl Cancer Inst,2015

2. Pheochromocytoma and paraganglioma pathogenesis: learning from genetic heterogeneity;Dahia;Nat Rev Cancer,2014

3. High prevalence of founder mutations of the succinate dehydrogenase genes in the Netherlands;Hensen;Clin Genet,2012

4. Tumour risks and genotype-phenotype analysis in 358 patients with germline mutations in SDHB and SDHD;Ricketts;Hum Mutat,2010

5. Clinical predictors for germline mutations in head and neck paraganglioma patients: cost reduction strategy in genetic diagnosis process and fall-out;Neumann;Cancer Res,2009

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