Results
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3541.
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3542.
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3543.
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3544.
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An alternative approach to establishing unbiased colorectal cancer risk estimation in Lynch syndrome. [electronic resource] by
- Suerink, Manon
- Rodríguez-Girondo, Mar
- van der Klift, Heleen M
- Colas, Chrystelle
- Brugieres, Laurence
- Lavoine, Noémie
- Jongmans, Marjolijn
- Munar, Gabriel Capellá
- Evans, D Gareth
- Farrell, Michael P
- Genuardi, Maurizio
- Goldberg, Yael
- Gomez-Garcia, Encarna
- Heinimann, Karl
- Hoell, Jessica I
- Aretz, Stefan
- Jasperson, Kory W
- Kedar, Inbal
- Modi, Mitul B
- Nikolaev, Sergey
- van Os, Theo A M
- Ripperger, Tim
- Rueda, Daniel
- Senter, Leigha
- Sjursen, Wenche
- Sunde, Lone
- Therkildsen, Christina
- Tibiletti, Maria G
- Trainer, Alison H
- Vos, Yvonne J
- Wagner, Anja
- Winship, Ingrid
- Wimmer, Katharina
- Zimmermann, Stefanie Y
- Vasen, Hans F
- van Asperen, Christi J
- Houwing-Duistermaat, Jeanine J
- Ten Broeke, Sanne W
- Nielsen, Maartje
Producer: 20200501
In:
Genetics in medicine : official journal of the American College of Medical Genetics vol. 21
Availability: No items available.
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3545.
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3546.
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Dietary factors, genetic susceptibility and somatic mutations in colorectal cancer: a prospective study. [electronic resource] by
- Weijenberg, M P
- Brink, M
- Lüchtenborg, M
- Wark, P A
- de Goeij, A F P M
- de Bruïne, A P
- van't Veer, P
- Kampman, E
- van Muijen, G N P
- Goldbohm, R A
- van den Brandt, P A
Producer: 20030430
In:
IARC scientific publications vol. 156
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3547.
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3548.
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Undectable expression of hMLH1 protein in sporadic colorectal cancer with replication error phenotype. [electronic resource] by
- Koike, J
- Yamada, K
- Takano, S
- Kikuchi, Y
- Hemmi, H
- Koi, M
- Tsujita, K
- Yanagita, K
- Yoshio, T
- Shimatake, H
Producer: 19971107
In:
Diseases of the colon and rectum vol. 40
Availability: No items available.
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3549.
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Mutations of two PMS homologues in hereditary nonpolyposis colon cancer. [electronic resource] by
- Nicolaides, N C
- Papadopoulos, N
- Liu, B
- Wei, Y F
- Carter, K C
- Ruben, S M
- Rosen, C A
- Haseltine, W A
- Fleischmann, R D
- Fraser, C M
Producer: 19940923
In:
Nature vol. 371
Availability: No items available.
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3550.
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3551.
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3552.
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3553.
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A genetic model for determining MSH2 and MLH1 carrier probabilities based on family history and tumor microsatellite instability. [electronic resource] by
- Marroni, F
- Pastrello, C
- Benatti, P
- Torrini, M
- Barana, D
- Cordisco, E L
- Viel, A
- Mareni, C
- Oliani, C
- Genuardi, M
- Bailey-Wilson, J E
- Ponz de Leon, M
- Presciuttini, S
Producer: 20060525
In:
Clinical genetics vol. 69
Availability: No items available.
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3554.
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The inframe MSH2 codon 596 deletion is linked with HNPCC and associated with lack of MSH2 protein in tumours. [electronic resource] by
- Stormorken, Astrid T
- Müller, Wolfram
- Lindblom, Annika
- Heimdal, Ketil
- Aase, Steinar
- Lothe, Inger Marie Bowitz
- Norèn, Tove
- Wijnen, Juul T
- Möslein, Gabriela
- Møller, Pål
Producer: 20031216
In:
Familial cancer vol. 2
Availability: No items available.
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3557.
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3560.
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