Results
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3581.
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3582.
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3583.
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Family history characteristics, tumor microsatellite instability and germline MSH2 and MLH1 mutations in hereditary colorectal cancer. [electronic resource] by
- Bapat, B V
- Madlensky, L
- Temple, L K
- Hiruki, T
- Redston, M
- Baron, D L
- Xia, L
- Marcus, V A
- Soravia, C
- Mitri, A
- Shen, W
- Gryfe, R
- Berk, T
- Chodirker, B N
- Cohen, Z
- Gallinger, S
Producer: 19990420
In:
Human genetics vol. 104
Availability: No items available.
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3584.
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3585.
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3586.
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3587.
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An MLH1 haplotype is over-represented on chromosomes carrying an HNPCC predisposing mutation in MLH1. [electronic resource] by
- 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
Producer: 20020528
In:
Journal of medical genetics vol. 39
Availability: No items available.
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3588.
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3589.
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3590.
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3591.
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3592.
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Challenges and pitfalls in HNPCC screening by microsatellite analysis and immunohistochemistry. [electronic resource] by
- Müller, Annegret
- Giuffre, Giuseppe
- Edmonston, Tina Bocker
- Mathiak, Micaela
- Roggendorf, Beate
- Heinmöller, Ernst
- Brodegger, Thomas
- Tuccari, Giovanni
- Mangold, Elisabeth
- Buettner, Reinhard
- Rüschoff, Josef
Producer: 20050422
In:
The Journal of molecular diagnostics : JMD vol. 6
Availability: No items available.
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3593.
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3594.
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Distinct patterns of KRAS mutations in colorectal carcinomas according to germline mismatch repair defects and hMLH1 methylation status. [electronic resource] by
- Oliveira, Carla
- Westra, Jantine L
- Arango, Diego
- Ollikainen, Miina
- Domingo, Enric
- Ferreira, Ana
- Velho, Sérgia
- Niessen, Renee
- Lagerstedt, Kristina
- Alhopuro, Pia
- Laiho, Paivi
- Veiga, Isabel
- Teixeira, Manuel R
- Ligtenberg, Marjolijn
- Kleibeuker, Jan H
- Sijmons, Rolf H
- Plukker, John T
- Imai, Kohzoh
- Lage, Pedro
- Hamelin, Richard
- Albuquerque, Cristina
- Schwartz, Simo
- Lindblom, Annika
- Peltomaki, Päivi
- Yamamoto, Hiroyuki
- Aaltonen, Lauri A
- Seruca, Raquel
- Hofstra, Robert M W
Producer: 20050217
In:
Human molecular genetics vol. 13
Availability: No items available.
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3595.
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MSH2 c.1452-1455delAATG is a founder mutation and an important cause of hereditary nonpolyposis colorectal cancer in the southern Chinese population. [electronic resource] by
- Chan, Tsun Leung
- Chan, Yee Wai
- Ho, Judy W C
- Chan, Celine
- Chan, Annie S Y
- Chan, Emily
- Lam, Polly W Y
- Tse, Chun Wah
- Lee, Kam Cheong
- Lau, Chi Waii
- Gwi, Elaine
- Leung, Suet Yi
- Yuen, Siu Tsan
Producer: 20040603
In:
American journal of human genetics vol. 74
Availability: No items available.
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3596.
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3597.
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3598.
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3599.
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3600.
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Characterization of a novel founder MSH6 mutation causing Lynch syndrome in the French Canadian population. [electronic resource] by
- Castellsagué, E
- Liu, J
- Volenik, A
- Giroux, S
- Gagné, R
- Maranda, B
- Roussel-Jobin, A
- Latreille, J
- Laframboise, R
- Palma, L
- Kasprzak, L
- Marcus, V A
- Breguet, M
- Nolet, S
- El-Haffaf, Z
- Australie, K
- Gologan, A
- Aleynikova, O
- Oros-Klein, K
- Greenwood, C
- Mes-Masson, A M
- Provencher, D
- Tischkowitz, M
- Chong, G
- Rousseau, F
- Foulkes, W D
Producer: 20160202
In:
Clinical genetics vol. 87
Availability: No items available.
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