Please use this identifier to cite or link to this item:
https://olympias.lib.uoi.gr/jspui/handle/123456789/22970| Title: | Combined genetic defect (homogeneity for factor V Leiden and heterogeneity for prothrombin G20210A allele), in a young patient, with recurrent deep vein thrombosis and serious postphlebitic syndrome--a case report |
| Institution and School/Department of submitter: | Πανεπιστήμιο Ιωαννίνων. Σχολή Επιστημών Υγείας. Τμήμα Ιατρικής |
| Keywords: | Adult,Factor V/*genetics,Heterozygote,Homozygote,Humans,Male,*Point Mutation,Postphlebitic Syndrome/*genetics,Prothrombin/*genetics,Recurrence,Venous Thrombosis/*genetics |
| URI: | https://olympias.lib.uoi.gr/jspui/handle/123456789/22970 |
| ISSN: | 0003-3197 |
| Link: | http://www.ncbi.nlm.nih.gov/pubmed/10779003 |
| Appears in Collections: | Άρθρα σε επιστημονικά περιοδικά ( Ανοικτά) - ΙΑΤ |
Files in This Item:
There are no files associated with this item.
This item is licensed under a Creative Commons License
