The Concise Handbook of Family Cancer Syndromes
Open Access
- 15 July 1998
- journal article
- review article
- Published by Oxford University Press (OUP) in JNCI Journal of the National Cancer Institute
- Vol. 90 (14) , 1039-1071
- https://doi.org/10.1093/jnci/90.14.1039
Abstract
Some details are inevitably lost when attempting to simplify subjects involving complex medical genetics subjects. However, unless an attempt is made to distill such topics, busy clinicians who may only occasionally need access to these subjects may perceive the information to be inaccessible. With these considerations in mind, we have attempted to develop a clinically usable catalog of recognizable family cancer syndromes. Thirtyfive different syndromes are included (shown in Tables 1-3). Thereafter, the subjects are listed in alphabetical order. For each disorder, the following template was used:Keywords
This publication has 181 references indexed in Scilit:
- Peutz-Jeghers syndrome is caused by mutations in a novel serine threoninekinaseNature Genetics, 1998
- The Risk of Cancer Associated with Specific Mutations ofBRCA1andBRCA2among Ashkenazi JewsNew England Journal of Medicine, 1997
- A Familial Syndrome of Pancreatic Cancer and Melanoma with a Mutation in theCDKN2Tumor-Suppressor GeneNew England Journal of Medicine, 1995
- Experience with multiple endocrine neoplasia type 1 screeningJournal of Internal Medicine, 1995
- Rothmund-Thomson syndrome with osteosarcomaJournal of the American Academy of Dermatology, 1993
- Rothmund-Thomson syndrome: Review of the world literaturePublished by Elsevier ,1992
- Risk of hepatoblastoma in familial adenomatous polyposisThe Journal of Pediatrics, 1991
- The International Collaborative Group on Hereditary Non-Polyposis Colorectal Cancer (ICG-HNPCC)Diseases of the Colon & Rectum, 1991
- Familial gastric cancer and immunologic abnormalitiesCancer, 1973
- Genetic studies of gastric cancer in humans: An appraisalCancer, 1958