Familial Papillary Thyroid Cancer—Many Syndromes, Too Many Genes?*-Reference-Cited by-同舟云学术

Familial Papillary Thyroid Cancer—Many Syndromes, Too Many Genes?*

Published:2000-05-01 Issue:5 Volume:85 Page:1755-1757
ISSN:0021-972X
Container-title:The Journal of Clinical Endocrinology & Metabolism
language:en
Short-container-title:

Author:

Eng Charis¹

Affiliation:

1. Clinical Cancer Genetics and Human Cancer Genetics Programs Ohio State University Comprehensive Cancer Center Columbus, Ohio 43210 and Cancer Research Campaign Human Cancer Genetics Research Group University of Cambridge Cambridge CB2 2QQ, United Kingdom

Publisher

The Endocrine Society

Subject

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

Link

http://academic.oup.com/jcem/article-pdf/85/5/1755/9057456/jcem1755.pdf

Reference12 articles.

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2. Statement of the American Society of Clinical Oncology—genetic testing for cancer susceptibility;Offit;J Clin Oncol.,1996

3. Mutation spectrum and genotype-phenotype analyses in Cowden disease and Bannayan-Zonana syndrome, two hamartoma syndromes with germline PTEN mutation;Marsh;Hum Mol Genet.,1998

4. Germline PTEN mutations in Cowden syndrome-like families;Marsh;J Med Genet.,1998

5. Familial papillary thyroid carcinoma is distinct from familial adenomatous polyposis coli;Malchoff;Thyroid.,1999

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2. Somatic Genomic Changes in the Formation of Differentiated Thyroid Carcinoma;Acta Medica Bulgarica;2020-09-01

3. Familial Papillary Thyroid Carcinoma (FPTC): a Retrospective Analysis in a Sample of the Bulgarian Population for a 10-Year Period;Endocrine Pathology;2016-10-22