SDHAF2 mutations in familial and sporadic paraganglioma and phaeochromocytoma
Top Cited Papers
- 1 April 2010
- journal article
- research article
- Published by Elsevier in The Lancet Oncology
- Vol. 11 (4) , 366-372
- https://doi.org/10.1016/s1470-2045(10)70007-3
Abstract
No abstract availableKeywords
This publication has 25 references indexed in Scilit:
- SDH5 , a Gene Required for Flavination of Succinate Dehydrogenase, Is Mutated in ParagangliomaScience, 2009
- The first Dutch SDHB founder deletion in paraganglioma – pheochromocytoma patientsBMC Medical Genetics, 2009
- Clinical Predictors for Germline Mutations in Head and Neck Paraganglioma Patients: Cost Reduction Strategy in Genetic Diagnostic Process as Fall-OutCancer Research, 2009
- IDH1andIDH2Mutations in GliomasNew England Journal of Medicine, 2009
- Worldwide Human Relationships Inferred from Genome-Wide Patterns of VariationScience, 2008
- Extra-adrenal and adrenal pheochromocytomas associated with a germline SDHC mutationNature Clinical Practice Endocrinology & Metabolism, 2008
- PLINK: A Tool Set for Whole-Genome Association and Population-Based Linkage AnalysesAmerican Journal of Human Genetics, 2007
- Genetic screening for pheochromocytoma: should SDHC gene analysis be included?Journal of Medical Genetics, 2007
- A Fast and Flexible Statistical Model for Large-Scale Population Genotype Data: Applications to Inferring Missing Genotypes and Haplotypic PhaseAmerican Journal of Human Genetics, 2006
- Haploview: analysis and visualization of LD and haplotype mapsBioinformatics, 2004