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발행년	- (예 : 2010-2015)

전체선택

An MLH1 haplotype is over-represented on chromosomes carrying an HNPCC predisposing mutation in MLH1

Academic Journal

Hutter, P; Wijnen, J; Rey-Berthod, C; Thiffault, I; Verkuijlen, P; Farber, D; Hamel, N; Bapat, B; Thibodeau, S N; Burn, J; Wu, J; MacNamara, E; Heinimann, K; Chong, G; Foulkes, W D

Journal of Medical Genetics. May 01, 2002 39(5):323-327

Full Text (BMJ Journals) Full Text (Gale Academic Onefile) Full Text (ProQuest Central) Full Text (Gale General Onefile) Web of Science JCR 저널정보 Scopus Find it@PNU

Specific and efficient targeting of adenovirus vectors to macrophages: application of a fusion protein between an adenovirus-binding fragment and avidin, linked to a biotinylated oligonucleotide

Academic Journal

Gras, JCE; Verkuijlen, P; Frants, RR; Havekes, LM; van Berkel, TJC; Biessen, EAL; van Dijk, KW

JOURNAL OF GENE MEDICINE; JUN 2006, 8 6, p668-p678, 11p.

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Cancer risk in hereditary nonpolyposis colorectal cancer due to MSH6 mutations: Impact on counseling and surveillance

Electronic Resource

Hendriks, Y; Wagner, A; Morreau, H; Menko, F; Stormorken, A; Quehenberger, F; Sandkuijl, L; Moller, P; Genuardi, Maurizio; Van Houwelingen, H; Tops, C; Van Puijenbroek, M; Verkuijlen, P; Kenter, G; Van Mil, A; Meijers-Heijboer, H; Tan, G; Breuning, M; Fodde, R; Wijnen, J; Brocker-Vriends, A; Vasen, H; Genuardi, M (ORCID:0000-0002-7410-8351)

Open Access (OAIster)

The CHEK2*1100delC mutation identifies families with a hereditary breast and colorectal cancer phenotype

Electronic Resource

Meijers-Heijboer, EJ; van Wijnen, J (Juul); Vasen, H; Wasielewski, M (Marijke); Wagner, Anja; Hollestelle, Antoinette; Elstrodt, F; Bos, Patrick; de Snoo, A; Tjon A Fat, G; Brekelmans, CTM (Cecile); Jagmohan, S; Franken, Patrick; Verkuijlen, P; van den Ouweland, Ans; Chapman, P; Tops, C; Möslein, G; Burn, J; Lynch, H; Klijn, Jan; Fodde, Riccardo; Schutte, Mieke

Meijers-Heijboer , EJ , van Wijnen , J , Vasen , H , Wasielewski , M , Wagner , A , Hollestelle , A , Elstrodt , F , Bos , P , de Snoo , A , Tjon A Fat , G , Brekelmans , CTM , Jagmohan , S , Franken , P , Verkuijlen , P , van den Ouweland , A , Chapman , P , Tops , C , Möslein , G , Burn , J , Lynch , H , Klijn , J , Fodde , R & Schutte , M 2003 , ' The CHEK2*1100delC mutation identifies families with a hereditary breast and colorectal cancer phenotype ' , American Journal of Human Genetics , vol. 72 , pp. 1308-1314 .

Open Access (OAIster)

Cancer risk in hereditary nonpolyposis colorectal cancer due to MSH6 mutations: Impact on counseling and surveillance

Academic Journal

Hendriks, YMC; Wagner, A; Morreau, H; Menko, F; Stormorken, A; Quehenberger, F; Sandkuijl, L; Moller, P; Genuardi, M; Van Houwelingen, H; Tops, C; Van Puijenbroek, M; Verkuijlen, P; Kenter, G; Van Mil, A; Meijers-Heijboer, H; Tan, GB; Breuning, MH; Fodde, R; Wijnen, JT; Brocker-Vriends, AHJT; Vasen, H

GASTROENTEROLOGY; JUL 2004, 127 1, p17-p25, 9p.

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The CHEK2 1100delC mutation identifies families with a hereditary breast and colorectal cancer phenotype

Academic Journal

Meijers-Heijboer, H; Wijnen, J; Vasen, H; Wasielewski, M; Wagner, A; Hollestelle, A; Elstrodt, F; van den Bos, R; de Snoo, A; Fat, GTA; Brekelmans, C; Jagmohan, S; Franken, P; Verkuijlen, P; van den Ouweland, A; Chapman, P; Tops, C; Moslein, G; Burn, J; Lynch, H; Klijn, J; Fodde, R; Schutte, M

AMERICAN JOURNAL OF HUMAN GENETICS; MAY 2003, 72 5, p1308-p1314, 7p.

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Molecular analysis of hereditary nonpolyposis colorectal cancer in the United States: High mutation detection rate among clinically selected families and characterization of an American founder genomic deletion of the MSH2 gene

Academic Journal

Wagner, A; Barrows, A; Wijnen, JT; van der Klift, H; Franken, PF; Verkuijlen, P; Nakagawa, H; Geugien, M; Jaghmohan-Changur, S; Breukel, C; Meijers-Heijboer, H; Morreau, H; van Puijenbroek, M; Burn, J; Coronel, S; Kinarski, Y; Okimoto, R; Watson, P; Lynch, JF; de la Chapelle, A; Lynch, HT; Fodde, R

AMERICAN JOURNAL OF HUMAN GENETICS; MAY 2003, 72 5, p1088-p1100, 13p.

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