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The nonsense mutation MSH2 c.2152C>T shows a founder effect in Portuguese Lynch syndrome families. [electronic resource] by
- Pinheiro, Manuela
- Francisco, Inês
- Pinto, Carla
- Peixoto, Ana
- Veiga, Isabel
- Filipe, Bruno
- Santos, Catarina
- Maia, Sofia
- Silva, João
- Pinto, Pedro
- Santos, Rui
- Claro, Isabel
- Lage, Pedro
- Lopes, Paula
- Ferreira, Sara
- Rosa, Isadora
- Fonseca, Ricardo
- Rodrigues, Paula
- Henrique, Rui
- Chaves, Paula
- Pereira, António Dias
- Brandão, Catarina
- Albuquerque, Cristina
- Teixeira, Manuel R
Producer: 20200109
In:
Genes, chromosomes & cancer vol. 58
Availability: No items available.
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Familial endometrial cancer in female carriers of MSH6 germline mutations. [electronic resource] by
- Wijnen, J
- de Leeuw, W
- Vasen, H
- van der Klift, H
- Møller, P
- Stormorken, A
- Meijers-Heijboer, H
- Lindhout, D
- Menko, F
- Vossen, S
- Möslein, G
- Tops, C
- Bröcker-Vriends, A
- Wu, Y
- Hofstra, R
- Sijmons, R
- Cornelisse, C
- Morreau, H
- Fodde, R
Producer: 19991019
In:
Nature genetics vol. 23
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Prevalence of the mismatch-repair-deficient phenotype in colonic adenomas arising in HNPCC patients: results of a 5-year follow-up study. [electronic resource] by
- Müller, Annegret
- Beckmann, Carmen
- Westphal, Gabriela
- Bocker Edmonston, Tina
- Friedrichs, Nicolaus
- Dietmaier, Wolfgang
- Brasch, Frank E
- Kloor, Matthias
- Poremba, Christoph
- Keller, Gisela
- Aust, Daniela E
- Fass, Jürgen
- Büttner, Reinhard
- Becker, Heinz
- Rüschoff, Josef
Producer: 20070201
In:
International journal of colorectal disease vol. 21
Availability: No items available.
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