Comprehensive mismatch repair gene panel identifies variants in patients with Lynch-like syndrome
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
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
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