Abstract
Guidelines for the establishment of an HNPCC register are presented. The aims of a register are discussed. Steps in identification of families and persons at risk are suggested, and possible sources of family and pedigree data are mentioned. The role of a register in surveillance, information of family members and medical colleagues, research and international collaboration are discussed.
| Originalsprog | Engelsk |
|---|---|
| Tidsskrift | Anticancer Research |
| Vol/bind | 14 |
| Udgave nummer | 4 B |
| Sider (fra-til) | 1647-1650 |
| Antal sider | 4 |
| ISSN | 0250-7005 |
| Status | Udgivet - 1994 |
| Udgivet eksternt | Ja |
Fingeraftryk
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