Identification of MEN1 and HRPT2 somatic mutations in paraffin-embedded (sporadic) parathyroid carcinomas.

Haven, C J; van Puijenbroek, M; Tan, M H; Teh, B T; Fleuren, G J; van Wezel, T; Morreau, H

Haven, C J; van Puijenbroek, M; Tan, M H; Teh, B T; Fleuren, G J; van Wezel, T; Morreau, H.

Affiliation

Haven CJ; Department of Pathology, Leiden University Medical Centre, The Netherlands.

Clin Endocrinol (Oxf) ; 67(3): 370-6, 2007 Sep.

Article in En | MEDLINE | ID: mdl-17555500

Subject(s)

Multiple Endocrine Neoplasia Type 1/genetics; Parathyroid Neoplasms/genetics; Proto-Oncogene Proteins/genetics; Tumor Suppressor Proteins/genetics; Adult; Aged; Aged, 80 and over; Biological Specimen Banks; Cohort Studies; DNA Mutational Analysis; Female; Frameshift Mutation; Humans; Loss of Heterozygosity/genetics; Male; Middle Aged; Multiple Endocrine Neoplasia Type 1/pathology; Mutation, Missense; Netherlands; Paraffin Embedding; Parathyroid Neoplasms/pathology

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Collection: 01-internacional Database: MEDLINE Main subject: Parathyroid Neoplasms / Proto-Oncogene Proteins / Multiple Endocrine Neoplasia Type 1 / Tumor Suppressor Proteins Type of study: Diagnostic_studies / Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Country/Region as subject: Europa Language: En Journal: Clin Endocrinol (Oxf) Year: 2007 Document type: Article Affiliation country: Netherlands Country of publication: United kingdom

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