Genome-Wide Copy Number Imbalances Identified in Familial and Sporadic Medullary Thyroid Carcinoma

Author:

Marsh Deborah J.12,Theodosopoulos George2,Martin-Schulte Klaus3,Richardson Anne-Louise12,Philips Jeanette45,Röher Hans-Dietrich3,Delbridge Leigh6,Robinson Bruce G.127

Affiliation:

1. Cancer Genetics (D.J.M., G.T., A.-L.R., B.G.R.), New South Wales 2065, Australia;

2. Departments of Molecular Medicine (D.J.M., G.T., A.-L.R., B.G.R.), New South Wales 2006, Australia;

3. Department of General and Trauma Surgery (K.M.-S., H.-D.R.), Heinrich-Heine University, 40225 Düsseldorf, Germany

4. Kolling Institute of Medical Research, and Pacific Laboratory Medicine Services, Departments of Anatomical Pathology (J.P.), New South Wales 2065, Australia;

5. Pathology (J.P.), New South Wales 2006, Australia;

6. Surgery (L.D.), Royal North Shore Hospital, St. Leonards, New South Wales 2065, Australia;

7. Medicine (B.G.R.), University of Sydney, New South Wales 2006, Australia;

Publisher

The Endocrine Society

Subject

Biochemistry, medical,Clinical Biochemistry,Endocrinology,Biochemistry,Endocrinology, Diabetes and Metabolism

Reference33 articles.

1. Genetic insights into familial cancers—update and recent discoveries.;Marsh;Cancer Lett,2002

2. RET proto-oncogene mutations in multiple endocrine neoplasia type 2 and medullary thyroid carcinoma.;Marsh;Horm Res,1997

3. Somatic mutations in the RET proto-oncogene in sporadic medullary thyroid carcinoma.;Marsh;Clin Endocrinol,1996

4. Mutations of codon 918 in the RET proto-oncogene correlate to poor prognosis in sporadic medullary thyroid carcinomas.;Zedenius;J Clin Endocrinol Metab,1995

5. CGH alterations in medullary thyroid carcinomas in relation to the RET M918T mutation and clinical outcome.;Frisk;Int J Oncol,2001

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