Zobrazeno 1 - 10
of 31
pro vyhledávání: '"Tom G.W. Letteboer"'
Autor:
Jan Loeffen, Saskia M. J. Hopman, Natasha K. A. van Eijkelenburg, Cora M. Aalfs, Fonnet E. Bleeker, Lieke P.V. Berger, Peter Hammond, Floor A. M. Postema, Charlotte J. Dommering, Jakob K. Anninga, Janna A. Hol, Raoul C.M. Hennekam, Anja Wagner, Maran J. W. Olderode-Berends, Marry M. van den Heuvel-Eibrink, Tom G.W. Letteboer, Lisethe Meijer, Johannes H. M. Merks, Corianne A. J. M. de Borgie, Wijnanda A. Kors
Publikováno v:
Familial Cancer, 20, 263-271. SPRINGER
Familial Cancer
Familial Cancer, 20(4), 263-271. Springer Netherlands
Postema, F A M, Hopman, S M J, de Borgie, C A J M, Aalfs, C M, Anninga, J K, Berger, L P V, Bleeker, F E, Dommering, C J, van Eijkelenburg, N K A, Hammond, P, van den Heuvel-Eibrink, M M, Hol, J A, Kors, W A, Letteboer, T G W, Loeffen, J L C M, Meijer, L, Olderode-Berends, M J W, Wagner, A, Hennekam, R C & Merks, J H M 2021, ' Clinical value of a screening tool for tumor predisposition syndromes in childhood cancer patients (TuPS) : a prospective, observational, multi-center study ', Familial Cancer, vol. 20, no. 4, pp. 263-271 . https://doi.org/10.1007/s10689-021-00237-1
Familial Cancer
Familial Cancer, 20(4), 263-271. Springer Netherlands
Postema, F A M, Hopman, S M J, de Borgie, C A J M, Aalfs, C M, Anninga, J K, Berger, L P V, Bleeker, F E, Dommering, C J, van Eijkelenburg, N K A, Hammond, P, van den Heuvel-Eibrink, M M, Hol, J A, Kors, W A, Letteboer, T G W, Loeffen, J L C M, Meijer, L, Olderode-Berends, M J W, Wagner, A, Hennekam, R C & Merks, J H M 2021, ' Clinical value of a screening tool for tumor predisposition syndromes in childhood cancer patients (TuPS) : a prospective, observational, multi-center study ', Familial Cancer, vol. 20, no. 4, pp. 263-271 . https://doi.org/10.1007/s10689-021-00237-1
Recognizing a tumor predisposition syndrome (TPS) in a child with cancer is of clinical relevance. Earlier we developed a screening tool to increase diagnostic accuracy and clinical efficiency of identifying TPSs in children with cancer. Here we repo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::67cce1624134f5a9b26b091ecb172ecd
https://doi.org/10.1007/s10689-021-00237-1
https://doi.org/10.1007/s10689-021-00237-1
Autor:
Noah c. Helderman, Anne-Sophie Van Der Werf-’T Lam, Hans Morreau, Arnoud Boot, Tom Van Wezel, Maartje Nielsen, Diantha Terlouw, Sanne W. Bajwa-ten Broeke, Mar Rodríguez-Girondo, Demi van Egmond, Alexandra M.J. Langers, Monique E. van Leerdam, Emily Rayner, Christi J. van Asperen, Liselotte P. van Hest, Hans J.P. Gille, Floor A.M. Duijkers, Anja Wagner, Ellis L. Eikenboom, Tom G.W. Letteboer, Mirjam M. de Jong, Fonnet E. Bleeker, Encarna B. Gomez Garcìa, Manon Suerink, Carli M. Tops, Niels de Wind
Publikováno v:
MSH6 TUMOR GROUP 2023, ' Molecular Profile of MSH6-Associated Colorectal Carcinomas Shows Distinct Features From Other Lynch Syndrome–Associated Colorectal Carcinomas ', Gastroenterology, vol. 165, no. 1, pp. 271-274.e2 . https://doi.org/10.1053/j.gastro.2023.03.198
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1acb9f5b21ff316ff9b4e61fd4dd4b08
http://www.scopus.com/inward/record.url?scp=85160215499&partnerID=8YFLogxK
http://www.scopus.com/inward/record.url?scp=85160215499&partnerID=8YFLogxK
Autor:
Marjolijn C.J. Jongmans, Junxiao Zhang, Roland P. Kuiper, Nicoline Hoogerbrugge, Marjolijn J.L. Ligtenberg, Richarda M. De Voer, Arjen R. Mensenkamp, Ad Geurts van Kessel, Liesbeth Spruijt, C. Marleen Kets, Wendy A.G. van Zelst-Stam, Meyke I. Schouten, Marijke R. Wevers, Maran J.W. Olderode-Berends, Jan C. Oosterwijk, Marrit M. Hitzert, Tom G.W. Letteboer, Snežana Stanković, Eveline J. Kamping, Laurensia Yuniati, Frank N. van Leeuwen, Jürgen Weitz, Rachel S. van der Post, Manuel R. Teixeira, Huanliang Liu, Jianping Wang
Publikováno v:
Gastroenterology, 162, 969-974.e6
Gastroenterology, 162, 3, pp. 969-974.e6
Gastroenterology, 162, 3, pp. 969-974.e6
Contains fulltext : 248373.pdf (Publisher’s version ) (Open Access)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d7a3a2b35bd024ee71c1ce393dba73f0
https://doi.org/10.1053/j.gastro.2021.11.009
https://doi.org/10.1053/j.gastro.2021.11.009
Autor:
Lisa Elze, Arjen R. Mensenkamp, Iris D. Nagtegaal, Wendy A.G. van Zelst-Stams, Richarda M. de Voer, Marjolijn J.L. Ligtenberg, Charlotte J. Dommering, Nicoline Hoogerbrugge, Mirjam M. de Jong, Fonnet E. Bleeker, Edward M. Leter, Tom G.W. Letteboer, Maartje Nielsen, Rachel S. van der Post, Brigit Wapstra
Publikováno v:
Dutch LS-Like Study Group 2021, ' Somatic Nonepigenetic Mismatch Repair Gene Aberrations Underly Most Mismatch Repair–Deficient Lynch-Like Tumors ', Gastroenterology, vol. 160, no. 4, pp. 1414-1416.e3 . https://doi.org/10.1053/j.gastro.2020.11.042
Gastroenterology, 160, 4, pp. 1414-1416.e3
Gastroenterology, 160, 1414-1416.e3
Gastroenterology, 160, 4, pp. 1414-1416.e3
Gastroenterology, 160, 1414-1416.e3
Contains fulltext : 231707.pdf (Publisher’s version ) (Open Access)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6a6d37d7fca938eb321ef59c4b32d4d3
https://research.vumc.nl/en/publications/37d763d2-9179-46a1-8ab4-5da52167446c
https://research.vumc.nl/en/publications/37d763d2-9179-46a1-8ab4-5da52167446c
Autor:
Stefan Aretz, Jenny von Salomé, Liesbeth Spruijt, Inge Bernstein, Tom G.W. Letteboer, Theo A. M. van Os, Kristina Lagerstedt-Robinson, Magnus von Knebel Doeberitz, Encarna B. Gomez-Garcia, Verena Steinke-Lange, Sanne W. ten Broeke, Maran J. W. Olderode-Berends, Hans K. Schackert, Marta Pineda, Manon Suerink, Gabriel Capellá, Nils Rahner, Carli M. J. Tops, Mar Rodríguez-Girondo, Christoph Engel, Anja Wagner, Pål Møller, Liselotte P. van Hest, Maartje Nielsen
Publikováno v:
Ten Broeke, S W, Rodríguez-Girondo, M, Suerink, M, Aretz, S, Bernstein, I, Capella, G, Engel, C, Gomez-Garcia, E B, van Hest, L P, von Knebel Doeberitz, M, Lagerstedt-Robinson, K, Letteboer, T G W, Møller, P, van Os, T A M, Pineda, M, Rahner, N, Olderode-Berends, M J W, von Salomé, J, Schackert, H K, Spruijt, L, Steinke-Lange, V, Wagner, A, Tops, C M J & Nielsen, M 2019, ' The apparent genetic anticipation in PMS2-associated Lynch syndrome families is explained by birth cohort effect ', Cancer Epidemiology, Biomarkers & Prevention, vol. 28, no. 6, pp. 1010-1014 . https://doi.org/10.1158/1055-9965.EPI-18-0576
Cancer Epidemiology, Biomarkers & Prevention, 28, 6, pp. 1010-1014
Cancer Epidemiology, Biomarkers and Prevention, 28(6), 1010-1014
CANCER EPIDEMIOLOGY BIOMARKERS & PREVENTION, 28(6), 1010-1014. AMER ASSOC CANCER RESEARCH
Cancer Epidemiology Biomarkers and Prevention, 28(6), 1010-1014. American Association for Cancer Research Inc.
Cancer Epidemiology Biomarkers & Prevention, 28(6), 1010-1014. American Association for Cancer Research Inc.
Cancer epidemiology, biomarkers & prevention, 28(6), 1010-1014. American Association for Cancer Research Inc.
Cancer Epidemiology, Biomarkers and Prevention, 28(6), 1010-1014. AMER ASSOC CANCER RESEARCH
Cancer Epidemiology, Biomarkers & Prevention, 28, 1010-1014
ten Broeke, S W, Rodríguez-Girondo, M, Suerink, M, Aretz, S, Bernstein, I, Capella, G, Engel, C, Gomez-Garcia, E B, van Hest, L P, von Knebel Doeberitz, M, Lagerstedt-Robinson, K, Letteboer, T G W, Moller, P, van Os, T A, Pineda, M, Rahner, N, Olderode-Berends, M J W, von Salome, J, Schackert, H K, Spruijt, L, Steinke-Lange, V, Wagner, A, Tops, C M J & Nielsen, M 2019, ' The apparent genetic anticipation in PMS2-associated lynch syndrome families is explained by birth-cohort effect ', Cancer Epidemiology Biomarkers and Prevention, vol. 28, no. 6, pp. 1010-1014 . https://doi.org/10.1158/1055-9965.EPI-18-0576
Cancer Epidemiology, Biomarkers & Prevention, 28, 6, pp. 1010-1014
Cancer Epidemiology, Biomarkers and Prevention, 28(6), 1010-1014
CANCER EPIDEMIOLOGY BIOMARKERS & PREVENTION, 28(6), 1010-1014. AMER ASSOC CANCER RESEARCH
Cancer Epidemiology Biomarkers and Prevention, 28(6), 1010-1014. American Association for Cancer Research Inc.
Cancer Epidemiology Biomarkers & Prevention, 28(6), 1010-1014. American Association for Cancer Research Inc.
Cancer epidemiology, biomarkers & prevention, 28(6), 1010-1014. American Association for Cancer Research Inc.
Cancer Epidemiology, Biomarkers and Prevention, 28(6), 1010-1014. AMER ASSOC CANCER RESEARCH
Cancer Epidemiology, Biomarkers & Prevention, 28, 1010-1014
ten Broeke, S W, Rodríguez-Girondo, M, Suerink, M, Aretz, S, Bernstein, I, Capella, G, Engel, C, Gomez-Garcia, E B, van Hest, L P, von Knebel Doeberitz, M, Lagerstedt-Robinson, K, Letteboer, T G W, Moller, P, van Os, T A, Pineda, M, Rahner, N, Olderode-Berends, M J W, von Salome, J, Schackert, H K, Spruijt, L, Steinke-Lange, V, Wagner, A, Tops, C M J & Nielsen, M 2019, ' The apparent genetic anticipation in PMS2-associated lynch syndrome families is explained by birth-cohort effect ', Cancer Epidemiology Biomarkers and Prevention, vol. 28, no. 6, pp. 1010-1014 . https://doi.org/10.1158/1055-9965.EPI-18-0576
Background: PMS2-associated Lynch syndrome is characterized by a relatively low colorectal cancer penetrance compared with other Lynch syndromes. However, age at colorectal cancer diagnosis varies widely, and a strong genetic anticipation effect has
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0beddab517e53f3ad2c205e858456c07
https://vbn.aau.dk/da/publications/40c915a4-1b63-4f9e-a656-f8d3d59aa08f
https://vbn.aau.dk/da/publications/40c915a4-1b63-4f9e-a656-f8d3d59aa08f
Autor:
Maartje Nielsen, Marjolijn J. L. Ligtenberg, Yvonne Tiersma, Juul T. Wijnen, Maran J. W. Olderode-Berends, Encarna Gomez Garcia, B. Redeker, José B. M. Zonneveld, Sanne W. ten Broeke, Frederik J. Hes, Carli M. J. Tops, Peter Devilee, Theo A. M. van Os, Christi J. van Asperen, Hans J. J. P. Gille, Niels de Wind, Heleen M. van der Klift, Arjen R. Mensenkamp, Tom G.W. Letteboer, Yvonne J. Vos, Elsa C. Bik, Mark Drost, S. Verhoef, Liselotte P. van Hest, Anja Wagner
Publikováno v:
Human mutation, 37(11), 1162-1179. Wiley-Liss Inc.
Human Mutation, 37(11), 1162-1179. Wiley-Liss Inc.
Human Mutation, 37(11), 1162–1179. Wiley-Liss Inc.
Human Mutation, 37(11), 1162-1179. Wiley
Human Mutation, 37(11), 1162-1179
Human Mutation, 37, 11, pp. 1162-1179
Human Mutation, 37, 1162-1179
van der Klift, H M, Mensenkamp, A R, Drost, M, Bik, E C, Vos, Y J, Gille, H J J P, Redeker, B E J W, Tiersma, Y, Zonneveld, J B M, Garcia, E G, Letteboer, T G W, Olderode-Berends, M J W, van Hest, L P, van Os, T A, Verhoef, S, Wagner, A, van Asperen, C J, Ten Broeke, S W, Hes, F J, de Wind, N, Nielsen, M, Devilee, P, Ligtenberg, M J L, Wijnen, J T & Tops, C M J 2016, ' Comprehensive Mutation Analysis of PMS2 in a Large Cohort of Probands Suspected of Lynch Syndrome or Constitutional Mismatch Repair Deficiency Syndrome ', Human Mutation, vol. 37, no. 11, pp. 1162-1179 . https://doi.org/10.1002/humu.23052
Human Mutation, 37(11), 1162-1179. Wiley-Liss Inc.
Human Mutation, 37(11), 1162–1179. Wiley-Liss Inc.
Human Mutation, 37(11), 1162-1179. Wiley
Human Mutation, 37(11), 1162-1179
Human Mutation, 37, 11, pp. 1162-1179
Human Mutation, 37, 1162-1179
van der Klift, H M, Mensenkamp, A R, Drost, M, Bik, E C, Vos, Y J, Gille, H J J P, Redeker, B E J W, Tiersma, Y, Zonneveld, J B M, Garcia, E G, Letteboer, T G W, Olderode-Berends, M J W, van Hest, L P, van Os, T A, Verhoef, S, Wagner, A, van Asperen, C J, Ten Broeke, S W, Hes, F J, de Wind, N, Nielsen, M, Devilee, P, Ligtenberg, M J L, Wijnen, J T & Tops, C M J 2016, ' Comprehensive Mutation Analysis of PMS2 in a Large Cohort of Probands Suspected of Lynch Syndrome or Constitutional Mismatch Repair Deficiency Syndrome ', Human Mutation, vol. 37, no. 11, pp. 1162-1179 . https://doi.org/10.1002/humu.23052
Monoallelic PMS2 germline mutations cause 5-15% of Lynch syndrome, a midlife cancer predisposition, whereas biallelic PMS2 mutations cause approximately 60% of constitutional MMR deficiency (CMMRD), a rare childhood cancer syndrome. Recently improved
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d0e47d3e18fe6f732f598289c985f991
https://doi.org/10.1002/humu.23052
https://doi.org/10.1002/humu.23052
Autor:
Liesbeth Spruijt, Encarna Gomez Garcia, Maartje Nielsen, Tom van Wezel, Maran J. W. Olderode-Berends, Ewout W. Steyerberg, Hans J. J. P. Gille, Liselot P. van Hest, Juul T. Wijnen, Lisa Pagan, Manon Suerink, Sanne W. ten Broeke, Carli M. J. Tops, Theo A. M. van Os, Arjen R. Mensenkamp, B. Redeker, Tom G.W. Letteboer, Yvonne J. Vos, Fadwa A. Elsayed, Lizet E. van der Kolk, Anja Wagner
Publikováno v:
Familial Cancer, 17(4), 507-515. Springer Netherlands
Familial Cancer, 17, 507-515
Ten Broeke, S W, Elsayed, F A, Pagan, L, Olderode-Berends, M J W, Garcia, E G, Gille, H J P, van Hest, L P, Letteboer, T G W, van der Kolk, L E, Mensenkamp, A R, van Os, T A, Spruijt, L, Redeker, B J W, Suerink, M, Vos, Y J, Wagner, A, Wijnen, J T, Steyerberg, E W, Tops, C M J, van Wezel, T & Nielsen, M 2018, ' SNP association study in PMS2-associated Lynch syndrome ', Familial Cancer, vol. 17, no. 4, pp. 507-515 . https://doi.org/10.1007/s10689-017-0061-3
Familial Cancer, 17(4), 507-515. SPRINGER
Familial Cancer
Familial cancer, 17(4), 507-515. Springer Netherlands
Familial Cancer, 17(4), 507. Springer Netherlands
Familial Cancer, 17(4), 507-515. Springer, Cham
Familial Cancer, 17(4), 507-515
Familial Cancer, 17, 4, pp. 507-515
Familial Cancer, 17, 507-515
Ten Broeke, S W, Elsayed, F A, Pagan, L, Olderode-Berends, M J W, Garcia, E G, Gille, H J P, van Hest, L P, Letteboer, T G W, van der Kolk, L E, Mensenkamp, A R, van Os, T A, Spruijt, L, Redeker, B J W, Suerink, M, Vos, Y J, Wagner, A, Wijnen, J T, Steyerberg, E W, Tops, C M J, van Wezel, T & Nielsen, M 2018, ' SNP association study in PMS2-associated Lynch syndrome ', Familial Cancer, vol. 17, no. 4, pp. 507-515 . https://doi.org/10.1007/s10689-017-0061-3
Familial Cancer, 17(4), 507-515. SPRINGER
Familial Cancer
Familial cancer, 17(4), 507-515. Springer Netherlands
Familial Cancer, 17(4), 507. Springer Netherlands
Familial Cancer, 17(4), 507-515. Springer, Cham
Familial Cancer, 17(4), 507-515
Familial Cancer, 17, 4, pp. 507-515
Lynch syndrome (LS) patients are at high risk of developing colorectal cancer (CRC). Phenotypic variability might in part be explained by common susceptibility loci identified in Genome Wide Association Studies (GWAS). Previous studies focused mostly
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9b7f654b58d61da072c7628164449a54
https://research.vumc.nl/en/publications/3333469a-41bd-4a3f-a348-7644d0e64a7b
https://research.vumc.nl/en/publications/3333469a-41bd-4a3f-a348-7644d0e64a7b
Autor:
Melanie Schrumpf, Nicoline Hoogerbrugge, Anja Wagner, Marry H. Nieuwenhuis, Juul T. Wijnen, Fred H. Menko, Encarna B. Gomez Garcia, Frederik J. Hes, Hans Morreau, Hans F. A. Vasen, Maartje Nielsen, Carli M. J. Tops, Dina Ruano, Petra E A Huijts, Tom G.W. Letteboer, J.L. Harryvan, Rolf H. Sijmons, Ellen Kampman, Tom van Wezel
Publikováno v:
JOURNAL OF MEDICAL GENETICS, 51(1), 55-60. BMJ PUBLISHING GROUP
Journal of Medical Genetics, 51(1), 55-60
Hes, F J, Ruano, D, Nieuwenhuis, M, Tops, C M, Schrumpf, M, Nielsen, M, Huijts, P E A, Wijnen, J T, Wagner, A, Garcia, E B G, Sijmons, R H, Menko, F H, Letteboer, T G W, Hoogerbrugge, N, Harryvan, J, Kampman, E, Morreau, H, Vasen, H F A & van Wezel, T 2014, ' Colorectal cancer risk variants on 11q23 and 15q13 are associated with unexplained adenomatous polyposis ', Journal of Medical Genetics, vol. 51, no. 1, pp. 55-60 . https://doi.org/10.1136/jmedgenet-2013-102000
Journal of Medical Genetics, 51(1), 55-60. BMJ Publishing Group
Journal of Medical Genetics, 51, 1, pp. 55-60
Journal of Medical Genetics 51 (2014) 1
Journal of Medical Genetics, 51, 55-60
Journal of Medical Genetics, 51(1), 55-60
Hes, F J, Ruano, D, Nieuwenhuis, M, Tops, C M, Schrumpf, M, Nielsen, M, Huijts, P E A, Wijnen, J T, Wagner, A, Garcia, E B G, Sijmons, R H, Menko, F H, Letteboer, T G W, Hoogerbrugge, N, Harryvan, J, Kampman, E, Morreau, H, Vasen, H F A & van Wezel, T 2014, ' Colorectal cancer risk variants on 11q23 and 15q13 are associated with unexplained adenomatous polyposis ', Journal of Medical Genetics, vol. 51, no. 1, pp. 55-60 . https://doi.org/10.1136/jmedgenet-2013-102000
Journal of Medical Genetics, 51(1), 55-60. BMJ Publishing Group
Journal of Medical Genetics, 51, 1, pp. 55-60
Journal of Medical Genetics 51 (2014) 1
Journal of Medical Genetics, 51, 55-60
Background Colorectal adenomatous polyposis is associated with a high risk of colorectal cancer (CRC) and is frequently caused by germline mutations in APC or MUTYH. However, in about 20-30% of patients no underlying gene defect can be identified. In
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::23784bc0b77decf589253432153b2e4a
https://doi.org/10.1136/jmedgenet-2013-102000
https://doi.org/10.1136/jmedgenet-2013-102000
Autor:
Verena Steinke, Nicoline Hoogerbrugge, Magnus von Knebel Doeberitz, Rolf H. Sijmons, Encarna B. Gomez Garcia, Markus Loeffler, Wolff Schmiegel, Elke Holinski-Feder, Reinhard Buettner, Frederik J. Hes, Christoph Engel, Hans K. Schackert, Nils Rahner, Gabriela Moeslein, Theo A. M. van Os, Fred H. Menko, Timm O. Goecke, Tom G.W. Letteboer, Irma Kluijt, Hans F. A. Vasen, Heike Goergens, Wolfgang Dietmaier, Peter Propping, Anja Wagner
Publikováno v:
Journal of Clinical Oncology, 30(35), 4409-4415. American Society of Clinical Oncology
Journal of Clinical Oncology, 30, 35, pp. 4409-15
Journal of Clinical Oncology, 30(35), 4409-4415. AMER SOC CLINICAL ONCOLOGY
Journal of clinical oncology, 30(35), 4409-4415. American Society of Clinical Oncology
Engel, C, Loeffler, M, Steinke, V, Rahner, N, Holinski-Feder, E, Dietmaier, W, Schackert, H K, Goergens, H, Doeberitz, M V, Goecke, T O, Schmiegel, W, Buettner, R, Moeslein, G, Letteboer, T G W, Garcia, E G, Hes, F J, Hoogerbrugge, N, Menko, F H, van Os, T A M, Sijmons, RH, Wagner, A, Kluijt, I, Propping, P & Vasen, H F A 2012, ' Risks of Less Common Cancers in Proven Mutation Carriers With Lynch Syndrome ', Journal of Clinical Oncology, vol. 30, no. 35, pp. 4409-4415 . https://doi.org/10.1200/JCO.2012.43.2278
Journal of Clinical Oncology, 30, 4409-15
Journal of Clinical Oncology, 30, 35, pp. 4409-15
Journal of Clinical Oncology, 30(35), 4409-4415. AMER SOC CLINICAL ONCOLOGY
Journal of clinical oncology, 30(35), 4409-4415. American Society of Clinical Oncology
Engel, C, Loeffler, M, Steinke, V, Rahner, N, Holinski-Feder, E, Dietmaier, W, Schackert, H K, Goergens, H, Doeberitz, M V, Goecke, T O, Schmiegel, W, Buettner, R, Moeslein, G, Letteboer, T G W, Garcia, E G, Hes, F J, Hoogerbrugge, N, Menko, F H, van Os, T A M, Sijmons, RH, Wagner, A, Kluijt, I, Propping, P & Vasen, H F A 2012, ' Risks of Less Common Cancers in Proven Mutation Carriers With Lynch Syndrome ', Journal of Clinical Oncology, vol. 30, no. 35, pp. 4409-4415 . https://doi.org/10.1200/JCO.2012.43.2278
Journal of Clinical Oncology, 30, 4409-15
Purpose Patients with Lynch syndrome are at high risk for colon and endometrial cancer, but also at an elevated risk for other less common cancers. The purpose of this retrospective cohort study was to provide risk estimates for these less common can
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2f25cd7e8aa57a5c598f691d60e4bfc9
https://research.rug.nl/en/publications/7d4d84be-11c9-49cb-bc84-b1d2a322def6
https://research.rug.nl/en/publications/7d4d84be-11c9-49cb-bc84-b1d2a322def6
Autor:
Jeanine J. Houwing-Duistermaat, Rolf H. Sijmons, Cora M. Aalfs, Nicoline Hoogerbrugge, Marry H. Nieuwenhuis, E. B. Gomez Garcia, Carli M. J. Tops, T. van Wezel, Senno Verhoef, Zeinab Ghorbanoghli, Fred H. Menko, Frederik J. Hes, Tom G.W. Letteboer, Hans F. A. Vasen, Shantie Jagmohan-Changur, Anja Wagner, Juul T. Wijnen
Publikováno v:
Familial Cancer, 15(4), 563-570. SPRINGER
Familial Cancer, 15(4), 563–570. Springer Netherlands
Familial cancer, 15(4), 563-570. Springer Netherlands
Familial Cancer
Familial Cancer, 15(4), 563-570. Springer Netherlands
Familial Cancer, 15, 4, pp. 563-70
Familial Cancer, 15, 563-70
Familial Cancer, 15(4), 563-570. Springer, Cham
Familial Cancer, 15(4), 563–570. Springer Netherlands
Familial cancer, 15(4), 563-570. Springer Netherlands
Familial Cancer
Familial Cancer, 15(4), 563-570. Springer Netherlands
Familial Cancer, 15, 4, pp. 563-70
Familial Cancer, 15, 563-70
Familial Cancer, 15(4), 563-570. Springer, Cham
Contains fulltext : 167193.pdf (Publisher’s version ) (Open Access) Familial adenomatous polyposis (FAP) is a dominantly inherited syndrome caused by germline mutations in the APC gene and characterized by the development of multiple colorectal ade
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::54b02251738806fa5aa1f1a8ee1d1856
https://dspace.library.uu.nl/handle/1874/346538
https://dspace.library.uu.nl/handle/1874/346538