Predisposing Germline Mutations in Young Patients With Squamous Cell Cancer of the Oral Cavity.

[1]  C. Ong,et al.  Mutational landscapes of tongue carcinoma reveal recurrent mutations in genes of therapeutic and prognostic relevance , 2015, Genome Medicine.

[2]  C. Stratakis,et al.  Pituitary adenoma with paraganglioma/pheochromocytoma (3PAs) and succinate dehydrogenase defects in humans and mice. , 2015, The Journal of clinical endocrinology and metabolism.

[3]  Eric D Wieben,et al.  Prevalence of CDKN2A mutations in pancreatic cancer patients: implications for genetic counseling , 2011, European Journal of Human Genetics.

[4]  Fiona Douglas,et al.  Tumor risks and genotype–phenotype–proteotype analysis in 358 patients with germline mutations in SDHB and SDHD , 2010, Human mutation.

[5]  P. Rosenberg,et al.  Cancer in dyskeratosis congenita. , 2009, Blood.

[6]  D. Raben,et al.  Poor prognosis in patients with stage I and II oral tongue squamous cell carcinoma , 2008, Cancer.

[7]  P. Rosenberg,et al.  Cancer in Fanconi anemia. , 2003, Blood.

[8]  B. Alter Cancer in Fanconi anemia, 1927–2001 , 2003, Cancer.

[9]  Robert W. Miller,et al.  Mutations in RECQL4 cause a subset of cases of Rothmund-Thomson syndrome , 1999, Nature Genetics.

[10]  M. O'sullivan,et al.  SDHB immunohistochemistry: a useful tool in the diagnosis of Carney–Stratakis and Carney triad gastrointestinal stromal tumors , 2011, Modern Pathology.

[11]  R. Schneider-Stock,et al.  Hereditary p16-Leiden mutation in a patient with multiple head and neck tumors. , 2003, American journal of human genetics.

[12]  J. Shah,et al.  High incidence of head and neck squamous cell carcinoma in patients with Fanconi anemia. , 2003, Archives of otolaryngology--head & neck surgery.