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Correction: Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants: findings from the Prospective Lynch Syndrome Database

Publikation: Bidrag til tidsskriftKommentar/debatForskningpeer review

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  1. Polygenic risk scores and breast and epithelial ovarian cancer risks for carriers of BRCA1 and BRCA2 pathogenic variants

    Publikation: Bidrag til tidsskriftTidsskriftartikelForskningpeer review

  2. Sequential targeted exome sequencing of 1001 patients affected by unexplained limb-girdle weakness

    Publikation: Bidrag til tidsskriftTidsskriftartikelForskningpeer review

  3. Noncardiac genetic predisposition in sudden infant death syndrome

    Publikation: Bidrag til tidsskriftTidsskriftartikelForskningpeer review

  1. The molecular profile of mucosal melanoma

    Publikation: Bidrag til tidsskriftTidsskriftartikelForskningpeer review

  2. Whole genome landscapes of uveal melanoma show an ultraviolet radiation signature in iris tumours

    Publikation: Bidrag til tidsskriftTidsskriftartikelForskningpeer review

  3. A rare missense variant in APC interrupts splicing and causes AFAP in two Danish families

    Publikation: Bidrag til tidsskriftTidsskriftartikelForskningpeer review

  4. New Pathogenic Germline Variants in Very Early Onset and Familial Colorectal Cancer Patients

    Publikation: Bidrag til tidsskriftTidsskriftartikelForskningpeer review

  • Mev Dominguez-Valentin
  • Julian R Sampson
  • Toni T Seppälä
  • Sanne W Ten Broeke
  • John-Paul Plazzer
  • Sigve Nakken
  • Christoph Engel
  • Stefan Aretz
  • Mark A Jenkins
  • Lone Sunde
  • Inge Bernstein
  • Gabriel Capella
  • Francesc Balaguer
  • Huw Thomas
  • D Gareth Evans
  • John Burn
  • Marc Greenblatt
  • Eivind Hovig
  • Wouter H de Vos Tot Nederveen Cappel
  • Rolf H Sijmons
  • Lucio Bertario
  • Maria Grazia Tibiletti
  • Giulia Martina Cavestro
  • Annika Lindblom
  • Adriana Della Valle
  • Francisco Lopez-Köstner
  • Nathan Gluck
  • Lior H Katz
  • Karl Heinimann
  • Carlos A Vaccaro
  • Reinhard Büttner
  • Heike Görgens
  • Elke Holinski-Feder
  • Monika Morak
  • Stefanie Holzapfel
  • Robert Hüneburg
  • Magnus von Knebel Doeberitz
  • Markus Loeffler
  • Nils Rahner
  • Hans K Schackert
  • Verena Steinke-Lange
  • Wolff Schmiegel
  • Deepak Vangala
  • Kirsi Pylvänäinen
  • Laura Renkonen-Sinisalo
  • John L Hopper
  • Aung Ko Win
  • Robert W Haile
  • Noralane M Lindor
  • Steven Gallinger
  • Loïc Le Marchand
  • Polly A Newcomb
  • Jane C Figueiredo
  • Stephen N Thibodeau
  • Karin Wadt
  • Christina Therkildsen
  • Henrik Okkels
  • Zohreh Ketabi
  • Leticia Moreira
  • Ariadna Sánchez
  • Miquel Serra-Burriel
  • Marta Pineda
  • Matilde Navarro
  • Ignacio Blanco
  • Kate Green
  • Fiona Lalloo
  • Emma J Crosbie
  • James Hill
  • Oliver G Denton
  • Ian M Frayling
  • Einar Andreas Rødland
  • Hans Vasen
  • Miriam Mints
  • Florencia Neffa
  • Patricia Esperon
  • Karin Alvarez
  • Revital Kariv
  • Guy Rosner
  • Tamara Alejandra Pinero
  • María Laura Gonzalez
  • Pablo Kalfayan
  • Douglas Tjandra
  • Ingrid M Winship
  • Finlay Macrae
  • Gabriela Möslein
  • Jukka-Pekka Mecklin
  • Maartje Nielsen
  • Pål Møller
Vis graf over relationer

The original version of this Article did not contain details of Dutch Cancer Society (DCS) funding (grant number UL 2017-8223) in the Acknowledgements section. This has now been corrected in both the PDF and HTML versions of the Article.

OriginalsprogEngelsk
TidsskriftGenetics in medicine : official journal of the American College of Medical Genetics
Vol/bind22
Udgave nummer9
Sider (fra-til)1569
Antal sider1
ISSN1098-3600
DOI
StatusUdgivet - sep. 2020

ID: 60546353