Recently characterized molecular events in uncommon gynaecological neoplasms and their clinical importance

Author:

Witkowski Leora12,McCluggage W Glenn3,Foulkes William D124

Affiliation:

1. Department of Human Genetics; Lady Davis Institute and Segal Cancer Centre; Jewish General Hospital; McGill University; Montreal QC Canada

2. Department of Medical Genetics; Lady Davis Institute and Segal Cancer Centre; Jewish General Hospital; McGill University; Montreal QC Canada

3. Department of Pathology; Belfast Health and Social Care Trust; Belfast UK

4. Department of Medical Genetics; Research Institute; McGill University Health Centre; Montreal QC Canada

Publisher

Wiley

Subject

General Medicine,Histology,Pathology and Forensic Medicine

Reference59 articles.

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3. Exome sequencing identifies MAX mutations as a cause of hereditary pheochromocytoma;Comino-Mendez;Nat. Genet.,2011

4. Somatic APC mosaicism: a frequent cause of familial adenomatous polyposis (FAP);Aretz;Hum. Mutat.,2007

5. Mutation of FOXL2 in granulosa-cell tumors of the ovary;Shah;N. Engl. J. Med.,2009

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