Comprehensive mismatch repair gene panel identifies variants in patients with Lynch-like syndrome
Use of multigene-panel identifies pathogenic variants in several CRC-predisposing genes in patients previously tested for Lynch Syndrome
- Hansen, Maren F., Johansen, Jostein, Sjursen, Wenche, Sylvander, Anna E., Bjørnevoll, Inga, Talseth-Palmer, Bente A., Lavik, Liss A. S., Xavier, Alexandre, Engebretsen, Lars F., Scott, Rodney J., Drabløs, Finn
Lynch syndrome mutation spectrum in New South Wales, Australia, including 55 novel mutations
Targeted next-generation sequencing of 22 mismatch repair genes identifies Lynch syndrome families
Are you sure you would like to clear your session, including search history and login status?