Zobrazeno 1 - 10
of 127
pro vyhledávání: '"Kluijt, Irma"'
Risk of colorectal and endometrial cancers in EPCAM deletion-positive Lynch syndrome: a cohort study
Autor:
Kempers, Marlies JE, Kuiper, Roland P, Ockeloen, Charlotte W, Chappuis, Pierre O, Hutter, Pierre, Rahner, Nils, Schackert, Hans K, Steinke, Verena, Holinski-Feder, Elke, Morak, Monika, Kloor, Matthias, Büttner, Reinhard, Verwiel, Eugene TP, van Krieken, J Han, Nagtegaal, Iris D, Goossens, Monique, van der Post, Rachel S, Niessen, Renée C, Sijmons, Rolf H, Kluijt, Irma, Hogervorst, Frans BL, Leter, Edward M, Gille, Johan JP, Aalfs, Cora M, Redeker, Egbert JW, Hes, Frederik J, Tops, Carli MJ, van Nesselrooij, Bernadette PM, van Gijn, Marielle E, García, Encarna B Gómez, Eccles, Diana M, Bunyan, David J, Syngal, Sapna, Stoffel, Elena M, Culver, Julie O, Palomares, Melanie R, Graham, Tracy, Velsher, Lea, Papp, Janos, Oláh, Edith, Chan, Tsun L, Leung, Suet Y, van Kessel, Ad Geurts, Kiemeney, Lambertus ALM, Hoogerbrugge, Nicoline, Ligtenberg, Marjolijn JL
Publikováno v:
In Lancet Oncology 2011 12(1):49-55
Autor:
Bleiker Eveline MA, Menko Fred H, Kluijt Irma, Taal Babs G, Gerritsma Miranda A, Wever Lidwina DV, Aaronson Neil K
Publikováno v:
Hereditary Cancer in Clinical Practice, Vol 5, Iss 2, Pp 59-66 (2007)
Abstract Background This study examined: (1) levels of cancer-specific distress more than one year after genetic counselling for hereditary nonpolyposis colorectal cancer (HNPCC); (2) associations between sociodemographic, clinical and psychosocial f
Externí odkaz:
https://doaj.org/article/51df4b7fc8e34248af81a493efa89c21
Autor:
van Riel Els, Ausems Margreet GEM, Hogervorst Frans BL, Kluijt Irma, van Gijn Marielle E, van Echtelt Jeanne, Scheidel-Jacobse Karen, Hennekam Eric FAM, Stulp Rein P, Vos Yvonne J, Offerhaus G Johan A, Menko Fred H, Gille Johan JP
Publikováno v:
Hereditary Cancer in Clinical Practice, Vol 8, Iss 1, p 7 (2010)
Abstract Background An unclassified variant (UV) in exon 1 of the MLH1 gene, c.112A > C, p.Asn38His, was found in six families who meet diagnostic criteria for Lynch syndrome. The pathogenicity of this variant was unknown. We aim to elucidate the pat
Externí odkaz:
https://doaj.org/article/7c2db00209d040ec8249a124e950c0ef
Autor:
Axwijk, Priscilla Helene1 P.H.Axwijk@amc.uva.nl, Kluijt, Irma1, de Jong, Daphne2, Gille, Hans3, Teertstra, Jelle4, Horenblas, Simon5
Publikováno v:
European Journal of Clinical Investigation. May2010, Vol. 40 Issue 5, p433-439. 7p. 2 Color Photographs, 1 Diagram, 1 Chart.
Autor:
van Steensel, Maurice *, Smith, Frances J.D. *, Steijlen, Peter M., Kluijt, Irma, Stevens, Howard P., Messenger, Andrew, Kremer, Hannie, Dunnill, M. Giles S., Kennedy, Cameron, Munro, Colin S., Doherty, Valerie R., McGrath, John A., Covello, Seana P., Coleman, Carrie M., Uitto, Jouni, McLean, W. H. Irwin **
Publikováno v:
In The American Journal of Human Genetics August 1999 65(2):413-419
Autor:
Jansen, Heike, van der Burg – Vermeulen, Sylvia, Schriemer, Arnold, Donker – Cools, Birgit, Schaafsma, Frederieke, Kluijt, Irma, Schouten, Lianne, Mazliah - de Vries, Marloes, Coffeng, Peter
Publikováno v:
Tijdschrift voor Bedrijfs- En Verzekeringsgeneeskunde; Oct2020, Vol. 28 Issue 9, p39-41, 3p
Autor:
Harinck, Femme1, Kluijt, Irma2, van Mil, Saskia E3, Waisfisz, Quinten3, van Os, Theo AM4, Aalfs, Cora M4, Wagner, Anja5, Olderode-Berends, Maran6, Sijmons, Rolf H6, Kuipers, Ernst J7, Poley, Jan-Werner1, Fockens, Paul8, Bruno, Marco J1
Publikováno v:
European Journal of Human Genetics. May2012, Vol. 20 Issue 5, p577-579. 3p. 3 Charts.
Akademický článek
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Akademický článek
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Large genomic deletions and duplications in the BRCA1 gene identified by a novel quantitative method
Autor:
Hogervorst, Frans B. L., Nederlof, Petra M., Gille, Johan J. P., McElgunn, Cathal J., Grippeling, Maartje, Pruntel, Roelof, Regnerus, Rein, van Welsem, Tibor, van Spaendonk, Resie, Menko, Fred H., Kluijt, Irma, Dommering, Charlotte, Verhoef, Senno, Schouten, Jan P., van't Veer, Laura J., Pals, Gerard
Publikováno v:
Cancer Research, 63(7), 1449-53. American Association for Cancer Research Inc.
Hogervorst, F B L, Nederlof, P M, Gille, J J P, McElgunn, C J, Grippeling, M, Pruntel, R, Regnerus, R, van Welsem, T, van Spaendonk, R, Menko, F H, Kluijt, I, Dommering, C, Verhoef, S, Schouten, J P, van't Veer, L J & Pals, G 2003, ' Large genomic deletions and duplications in the BRCA1 gene identified by a novel quantitative method ', Cancer Research, vol. 63, no. 7, pp. 1449-53 .
Cancer research, 63(7), 1449-1453. American Association for Cancer Research Inc.
Hogervorst, F B L, Nederlof, P M, Gille, J J P, McElgunn, C J, Grippeling, M, Pruntel, R, Regnerus, R, van Welsem, T, van Spaendonk, R, Menko, F H, Kluijt, I, Dommering, C, Verhoef, S, Schouten, J P, van't Veer, L J & Pals, G 2003, ' Large genomic deletions and duplications in the BRCA1 gene identified by a novel quantitative method ', Cancer Research, vol. 63, no. 7, pp. 1449-53 .
Cancer research, 63(7), 1449-1453. American Association for Cancer Research Inc.
We applied a novel method to detect single or multiple exon deletions and amplifications in the BRCA1 gene. The test, called multiplex ligation-dependent probe amplification (MLPA), uses probes designed to hybridize adjacently to the target sequence.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::c4550809006aa5968ccd31648db88cdc
https://research.vumc.nl/en/publications/fb3d5be9-99cd-45d6-8e48-bb2647401021
https://research.vumc.nl/en/publications/fb3d5be9-99cd-45d6-8e48-bb2647401021