Zobrazeno 1 - 8
of 8
pro vyhledávání: '"R. H. Sijmons"'
Autor:
L. F. Johansson, E. N. de Boer, H. A. de Weerd, F. van Dijk, M. G. Elferink, G. H. Schuring-Blom, R. F. Suijkerbuijk, R. J. Sinke, G. J. te Meerman, R. H. Sijmons, M. A. Swertz, B. Sikkema-Raddatz
Publikováno v:
Scientific Reports, Vol 7, Iss 1, Pp 1-11 (2017)
Abstract Non-invasive prenatal testing (NIPT) of cell-free DNA in maternal plasma, which is a mixture of maternal DNA and a low percentage of fetal DNA, can detect fetal aneuploidies using massively parallel sequencing. Because of the low percentage
Externí odkaz:
https://doaj.org/article/50fe59706dee446cb5379772bb6c48fa
Autor:
K. Bokkers, E. M. A. Bleiker, C. M. Aalfs, T. van Dalen, M. E. Velthuizen, P. Duijveman, R. H. Sijmons, W. Koole, E. J. P. Schoenmaeckers, M. G. E. M. Ausems
Publikováno v:
Annals of surgical oncology. SPRINGER
Background Pre-test genetic counseling for patients with breast cancer is increasingly being provided by nongenetic healthcare professionals. We evaluated the attitudes, knowledge, and self-efficacy of surgeons, oncologists, and nurses regarding main
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3e52e8f151dd6587495232bf4b3bcd29
https://research.rug.nl/en/publications/2ffc5d87-2e2e-47ea-9ace-ecc89a8d10a5
https://research.rug.nl/en/publications/2ffc5d87-2e2e-47ea-9ace-ecc89a8d10a5
Publikováno v:
The Journal of Urology. :466-470
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::183940e8346dd27008fe85fdf2aeaaf0
https://doi.org/10.1097/00005392-199808000-00048
https://doi.org/10.1097/00005392-199808000-00048
Autor:
C R M, Lammens, E M A, Bleiker, S, Verhoef, M G E M, Ausems, D, Majoor-Krakauer, R H, Sijmons, F J, Hes, E B, Gómez-García, T A M, Van Os, L, Spruijt, R B, van der Luijt, A M W, van den Ouweland, M W G, Ruijs, C, Gundy, T, Nagtegaal, N K, Aaronson
Publikováno v:
Psycho-oncology. 20(6)
Li Fraumeni syndrome (LFS) and Von Hippel-Lindau disease (VHL) are two rare hereditary tumor syndromes, characterized by a high risk of developing multiple tumors at various sites and ages for which preventive and treatment options are limited. For p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::f4e2447b970cc5f09251364bf1b62727
https://pubmed.ncbi.nlm.nih.gov/21384469
https://pubmed.ncbi.nlm.nih.gov/21384469
Autor:
Lucia I H, Overbeek, Nicoline, Hoogerbrugge, Joannes H J M, van Krieken, Fokko M, Nagengast, Theo J M, Ruers, Marjolijn J L, Ligtenberg, Rosella P M G, Hermens, R H, Sijmons
Publikováno v:
Diseases of the Colon and Rectum, 51, 8, pp. 1249-54
Diseases of the Colon and Rectum, 51, 1249-54
Diseases of the Colon and Rectum
Diseases of the Colon and Rectum, 51, 1249-54
Diseases of the Colon and Rectum
Contains fulltext : 70595.pdf (Publisher’s version ) (Open Access) PURPOSE: This study examined the referral process for genetic counseling at a cancer genetics clinic in patients with colorectal cancer and to search for determinants of variation i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::82378cffbe113231df9f357570fbd9f2
https://hdl.handle.net/2066/70595
https://hdl.handle.net/2066/70595
Autor:
R H, Sijmons, G T, Burger
Publikováno v:
Familial cancer. 1(1)
Cancer is associated with a wide range of hereditary disorders. Recognizing these disorders in cancer patients may be of great importance for the medical management of both patients and their relatives. Conversely, recognizing the fact that cancer ma
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::480a6359c514085964891ec707d750fc
https://pubmed.ncbi.nlm.nih.gov/14574016
https://pubmed.ncbi.nlm.nih.gov/14574016
Publikováno v:
Nederlands tijdschrift voor geneeskunde. 139(9)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::a3d10c88fafcea9c6049a4e0bbe2e9e9
https://pubmed.ncbi.nlm.nih.gov/7891763
https://pubmed.ncbi.nlm.nih.gov/7891763
Autor:
R. H. Sijmons
Publikováno v:
Familial Cancer Control ISBN: 9783642775840
Gebhardt discussed computerised Markov analysis as a tool to evaluate data on the occurrence of cancer in families registered at the Basel general cancer registry. Using this method in the study of first-degree relatives of probands with colorectal c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d1f2b15d9cf96996edeb6f3057c62789
https://doi.org/10.1007/978-3-642-77582-6_9
https://doi.org/10.1007/978-3-642-77582-6_9