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Published Erratum

. 2024 May;32(5):601-602.

doi: 10.1038/s41431-023-01519-1.

Publisher Correction: A 39 kb structural variant causing Lynch syndrome detected by optical genome mapping and nanopore sequencing

Pål Marius Bjørnstad^#¹, Ragnhild Aaløkken^#¹, June Åsheim^#¹, Arvind Y M Sundaram^#¹, Caroline N Felde¹, G Henriette Østby¹, Marianne Dalland¹, Wenche Sjursen², Christian Carrizosa¹, Magnus D Vigeland^{1

3}, Hanne S Sorte¹, Ying Sheng¹, Sarah L Ariansen¹, Eli Marie Grindedal^#¹, Gregor D Gilfillan^#⁴

Affiliations

Affiliations

¹ Department Medical Genetics, Oslo University Hospital and University of Oslo, Oslo, Norway.
² Department of Clinical & Molecular Medicine, NTNU and Department of Medical Genetics, St Olavs Hospital, Trondheim, Norway.
³ Department of Forensic Sciences, Oslo University Hospital, 0372, Oslo, Norway.
⁴ Department Medical Genetics, Oslo University Hospital and University of Oslo, Oslo, Norway. gregorg@medisin.uio.no.

^# Contributed equally.

PMID: 38172175
PMCID: PMC11061170
DOI: 10.1038/s41431-023-01519-1

Published Erratum

Publisher Correction: A 39 kb structural variant causing Lynch syndrome detected by optical genome mapping and nanopore sequencing

Pål Marius Bjørnstad et al. Eur J Hum Genet. 2024 May.

. 2024 May;32(5):601-602.

doi: 10.1038/s41431-023-01519-1.

Authors

Pål Marius Bjørnstad^#¹, Ragnhild Aaløkken^#¹, June Åsheim^#¹, Arvind Y M Sundaram^#¹, Caroline N Felde¹, G Henriette Østby¹, Marianne Dalland¹, Wenche Sjursen², Christian Carrizosa¹, Magnus D Vigeland^{1

3}, Hanne S Sorte¹, Ying Sheng¹, Sarah L Ariansen¹, Eli Marie Grindedal^#¹, Gregor D Gilfillan^#⁴

Affiliations

¹ Department Medical Genetics, Oslo University Hospital and University of Oslo, Oslo, Norway.
² Department of Clinical & Molecular Medicine, NTNU and Department of Medical Genetics, St Olavs Hospital, Trondheim, Norway.
³ Department of Forensic Sciences, Oslo University Hospital, 0372, Oslo, Norway.
⁴ Department Medical Genetics, Oslo University Hospital and University of Oslo, Oslo, Norway. gregorg@medisin.uio.no.

^# Contributed equally.

PMID: 38172175
PMCID: PMC11061170
DOI: 10.1038/s41431-023-01519-1

No abstract available

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Erratum for

A 39 kb structural variant causing Lynch Syndrome detected by optical genome mapping and nanopore sequencing.
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. Bjørnstad PM, et al. Eur J Hum Genet. 2024 May;32(5):513-520. doi: 10.1038/s41431-023-01494-7. Epub 2023 Nov 29. Eur J Hum Genet. 2024. PMID: 38030917 Free PMC article.

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