Bjørnstad PM, Aaløkken R, Åsheim J, Sundaram AYM, Felde CN, Østby GH, Dalland M, Sjursen W, Carrizosa C, Vigeland MD, Sorte HS, Sheng Y, Ariansen SL, Grindedal EM, Gilfillan GD(2024) Publisher Correction: A 39 kb structural variant causing Lynch syndrome detected by optical genome mapping and nanopore sequencing Eur J Hum Genet(in press) DOI 10.1038/s41431-023-01519-1, PubMed 38172175
Bjørnstad PM, Aaløkken R, Åsheim J, Sundaram AYM, Felde CN, Østby GH, Dalland M, Sjursen W, Carrizosa C, Vigeland MD, Sorte HS, Sheng Y, Ariansen SL, Grindedal EM, Gilfillan GD(2023) A 39 kb structural variant causing Lynch Syndrome detected by optical genome mapping and nanopore sequencing Eur J Hum Genet(in press) DOI 10.1038/s41431-023-01494-7, PubMed 38030917
Fantinato C, Fonneløp AE, Bleka Ø, Vigeland MD, Gill P(2023) The invisible witness: air and dust as DNA evidence of human occupancy in indoor premises Sci Rep, 13(1), 19059 DOI 10.1038/s41598-023-46151-7, PubMed 37925517
Get in touch
Magnus Dehli Vigeland: magnusdv@medisin.uio.no Visiting /postal address: Dept. Medical Genetics, Building 25, 1st floor (North), Ullevål Hospital, Kirkeveien 166, 0450 Oslo