Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Ineke Labrijn-Marks"'
Autor:
Clara Sá Miranda, Lies H. Hoefsloot, Karin Naess, Galhana M. Somers-Bolman, Ineke Labrijn-Marks, Irene Mavridou, Trijnie Dijkhuizen, Jasper J. Saris, Marianne Hoogeveen-Westerveld, Ans T. van der Ploeg, Frans W. Verheijen, Olga Amaral, Sirpa Ala-Mello, Hannerieke J. M. P. van den Hout, Dicky J. Halley, Helen Michelakakis, Stijn L.M. in 't Groen, W.W.M. Pim Pijnappel, Marloes Benjamins, M. A. Kroos
Publikováno v:
European Journal of Human Genetics
European Journal of Human Genetics, 27(6), 919-927. Nature Publishing Group
European Journal of Human Genetics, 27(6), 919-927. Nature Publishing Group
Collaboration from previous work institution. Free PMC article: https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/30737479/ Analyses in our diagnostic DNA laboratory include genes involved in autosomal recessive (AR) lysosomal storage disorders such as
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8345058af2e8178d27b294d6d11641e8
https://doi.org/10.1038/s41431-019-0348-y
https://doi.org/10.1038/s41431-019-0348-y
Autor:
Mieke Schutte, Jan G. M. Klijn, Ans M.W. van den Ouweland, Muhammad Riaz, Renske Olmer, Linda van der Spaa, Hanne Meijers-Heijboer, Ineke Labrijn-Marks, Joyce Vermeulen, Marijke Wasielewski, Dennis Dooijes
Publikováno v:
Breast cancer research and treatment, 123(2), 315-320. Springer New York
Breast Cancer Research and Treatment, 123(2), 315-320. Springer New York
Wasielewski, M, Riaz, M, Vermeulen, J, van den Ouweland, A, Labrijn-Marks, I, Olmer, R, van der Spaa, L, Klijn, J G M, Meijers-Heijboer, E J, Dooijes, D & Schutte, M 2010, ' Association of rare MSH6 variants with familial breast cancer ', Breast Cancer Research and Treatment, vol. 123, no. 2, pp. 315-320 . https://doi.org/10.1007/s10549-009-0634-4
Breast Cancer Research and Treatment, 123(2), 315-320. Springer New York
Wasielewski, M, Riaz, M, Vermeulen, J, van den Ouweland, A, Labrijn-Marks, I, Olmer, R, van der Spaa, L, Klijn, J G M, Meijers-Heijboer, E J, Dooijes, D & Schutte, M 2010, ' Association of rare MSH6 variants with familial breast cancer ', Breast Cancer Research and Treatment, vol. 123, no. 2, pp. 315-320 . https://doi.org/10.1007/s10549-009-0634-4
Germline mutations in the mismatch repair genes MLH1, MSH2, MSH6, and PMS2 predispose to Lynch syndrome (also known as hereditary non-polyposis colorectal cancer). Recently, we have shown that the CHEK2 1100delC mutation also is associated with Lynch
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0915e0d0cdaa72ce82d0095a00bc5731
https://pure.amc.nl/en/publications/association-of-rare-msh6-variants-with-familial-breast-cancer(25873bd9-6c24-4cb7-bc20-53aaf55a8a20).html
https://pure.amc.nl/en/publications/association-of-rare-msh6-variants-with-familial-breast-cancer(25873bd9-6c24-4cb7-bc20-53aaf55a8a20).html
