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4241.
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Mutational germline analysis of hMSH2 and hMLH1 genes in early onset colorectal cancer patients. [electronic resource] by
- Montera, M
- Resta, N
- Simone, C
- Guanti, G
- Marchese, C
- Civitelli, S
- Mancini, A
- Pozzi, S
- De Salvo, L
- Bruzzone, D
- Donadini, A
- Romio, L
- Mareni, C
Producer: 20000822
In:
Journal of medical genetics vol. 37
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4242.
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Atypical HNPCC owing to MSH6 germline mutations: analysis of a large Dutch pedigree. [electronic resource] by
- Wagner, A
- Hendriks, Y
- Meijers-Heijboer, E J
- de Leeuw, W J
- Morreau, H
- Hofstra, R
- Tops, C
- Bik, E
- Bröcker-Vriends, A H
- van Der Meer, C
- Lindhout, D
- Vasen, H F
- Breuning, M H
- Cornelisse, C J
- van Krimpen, C
- Niermeijer, M F
- Zwinderman, A H
- Wijnen, J
- Fodde, R
Producer: 20011018
In:
Journal of medical genetics vol. 38
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4243.
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4244.
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4245.
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Interpretation of immunohistochemistry for mismatch repair proteins is only reliable in a specialized setting. [electronic resource] by
- Overbeek, Lucia I H
- Ligtenberg, Marjolijn J L
- Willems, Riki W
- Hermens, Rosella P M G
- Blokx, Willeke A M
- Dubois, Stefan V
- van der Linden, Hans
- Meijer, Jos W R
- Mlynek-Kersjes, Maria L
- Hoogerbrugge, Nicoline
- Hebeda, Konnie M
- van Krieken, Joannes H J M
Producer: 20080814
In:
The American journal of surgical pathology vol. 32
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4246.
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4247.
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Implementation of universal microsatellite instability and immunohistochemistry screening for diagnosing lynch syndrome in a large academic medical center. [electronic resource] by
- Heald, Brandie
- Plesec, Thomas
- Liu, Xiuli
- Pai, Rish
- Patil, Deepa
- Moline, Jessica
- Sharp, Richard R
- Burke, Carol A
- Kalady, Matthew F
- Church, James
- Eng, Charis
Producer: 20130523
In:
Journal of clinical oncology : official journal of the American Society of Clinical Oncology vol. 31
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4248.
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4249.
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Early-onset colorectal cancer is an easy and effective tool to identify retrospectively Lynch syndrome. [electronic resource] by
- Perea, José
- Rodríguez, Yolanda
- Rueda, Daniel
- Marín, José C
- Díaz-Tasende, José
- Álvaro, Edurne
- Alegre, Cristina
- Osorio, Irene
- Colina, Francisco
- Lomas, Manuel
- Hidalgo, Manuel
- Benítez, Javier
- Urioste, Miguel
Producer: 20120207
In:
Annals of surgical oncology vol. 18
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4250.
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4251.
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Functional testing strategy for coding genetic variants of unclear significance in MLH1 in Lynch syndrome diagnosis. [electronic resource] by
- Hinrichsen, Inga
- Schäfer, Dieter
- Langer, Deborah
- Köger, Nicole
- Wittmann, Margarethe
- Aretz, Stefan
- Steinke, Verena
- Holzapfel, Stefanie
- Trojan, Jörg
- König, Rainer
- Zeuzem, Stefan
- Brieger, Angela
- Plotz, Guido
Producer: 20150424
In:
Carcinogenesis vol. 36
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4252.
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4253.
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4254.
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Cancer incidence and survival in Lynch syndrome patients receiving colonoscopic and gynaecological surveillance: first report from the prospective Lynch syndrome database. [electronic resource] by
- Møller, Pål
- Seppälä, Toni
- Bernstein, Inge
- Holinski-Feder, Elke
- Sala, Paola
- Evans, D Gareth
- Lindblom, Annika
- Macrae, Finlay
- Blanco, Ignacio
- Sijmons, Rolf
- Jeffries, Jacqueline
- Vasen, Hans
- Burn, John
- Nakken, Sigve
- Hovig, Eivind
- Rødland, Einar Andreas
- Tharmaratnam, Kukatharmini
- de Vos Tot Nederveen Cappel, Wouter H
- Hill, James
- Wijnen, Juul
- Green, Kate
- Lalloo, Fiona
- Sunde, Lone
- Mints, Miriam
- Bertario, Lucio
- Pineda, Marta
- Navarro, Matilde
- Morak, Monika
- Renkonen-Sinisalo, Laura
- Frayling, Ian M
- Plazzer, John-Paul
- Pylvanainen, Kirsi
- Sampson, Julian R
- Capella, Gabriel
- Mecklin, Jukka-Pekka
- Möslein, Gabriela
Producer: 20170707
In:
Gut vol. 66
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4255.
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Characterization of MSH2 and MLH1 mutations in Italian families with hereditary nonpolyposis colorectal cancer. [electronic resource] by
- Viel, A
- Genuardi, M
- Capozzi, E
- Leonardi, F
- Bellacosa, A
- Paravatou-Petsotas, M
- Pomponi, M G
- Fornasarig, M
- Percesepe, A
- Roncucci, L
- Tamassia, M G
- Benatti, P
- Ponz de Leon, M
- Valenti, A
- Covino, M
- Anti, M
- Foletto, M
- Boiocchi, M
- Neri, G
Producer: 19970310
In:
Genes, chromosomes & cancer vol. 18
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4256.
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Majority of hMLH1 mutations responsible for hereditary nonpolyposis colorectal cancer cluster at the exonic region 15-16. [electronic resource] by
- Wijnen, J
- Khan, P M
- Vasen, H
- Menko, F
- van der Klift, H
- van den Broek, M
- van Leeuwen-Cornelisse, I
- Nagengast, F
- Meijers-Heijboer, E J
- Lindhout, D
- Griffioen, G
- Cats, A
- Kleibeuker, J
- Varesco, L
- Bertario, L
- Bisgaard, M L
- Mohr, J
- Kolodner, R
- Fodde, R
Producer: 19960301
In:
American journal of human genetics vol. 58
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4257.
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Genetic linkage analysis in hereditary non-polyposis colon cancer syndrome. [electronic resource] by
- Froggatt, N J
- Koch, J
- Davies, R
- Evans, D G
- Clamp, A
- Quarrell, O W
- Weissenbach, J
- Hodgson, S V
- Ponder, B A
- Barton, D E
Producer: 19950823
In:
Journal of medical genetics vol. 32
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4258.
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4259.
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Mutator phenotype in Msh2-deficient murine embryonic fibroblasts. [electronic resource] by
- Reitmair, A H
- Risley, R
- Bristow, R G
- Wilson, T
- Ganesh, A
- Jang, A
- Peacock, J
- Benchimol, S
- Hill, R P
- Mak, T W
- Fishel, R
- Meuth, M
Producer: 19970924
In:
Cancer research vol. 57
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4260.
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