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3361.
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3362.
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3363.
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Spectrum and frequencies of mutations in MSH2 and MLH1 identified in 1,721 German families suspected of hereditary nonpolyposis colorectal cancer. [electronic resource] by
- Mangold, Elisabeth
- Pagenstecher, Constanze
- Friedl, Waltraut
- Mathiak, Micaela
- Buettner, Reinhard
- Engel, Christoph
- Loeffler, Markus
- Holinski-Feder, Elke
- Müller-Koch, Yvonne
- Keller, Gisela
- Schackert, Hans K
- Krüger, Stefan
- Goecke, Timm
- Moeslein, Gabriela
- Kloor, Matthias
- Gebert, Johannes
- Kunstmann, Erdmute
- Schulmann, Karsten
- Rüschoff, Josef
- Propping, Peter
Producer: 20050901
In:
International journal of cancer vol. 116
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3364.
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3365.
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3366.
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3367.
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3368.
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3369.
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3370.
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Germ line MLH1 and MSH2 mutations in Taiwanese Lynch syndrome families: characterization of a founder genomic mutation in the MLH1 gene. [electronic resource] by
- Tang, R
- Hsiung, C
- Wang, J-Y
- Lai, C-H
- Chien, H-T
- Chiu, L-L
- Liu, C-T
- Chen, H-H
- Wang, H-M
- Chen, S-X
- Hsieh, L-L
Producer: 20090722
In:
Clinical genetics vol. 75
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3371.
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3372.
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Retrorectal cystic hamartoma as benign cause of CA 19-9 elevation. [electronic resource] by
- Garcia-Donas, Jesus
- Rodriguez, Nuria
- Jara, Carlos
- Urioste, Miguel
- Nevado, Manuel
- Cañamero, Marta
- Cuartero, Victoria
- Albillos, Jose
- Vega, Daniel
- Quintans, Antonio
Producer: 20070911
In:
Journal of clinical oncology : official journal of the American Society of Clinical Oncology vol. 25
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3373.
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A ten markers panel provides a more accurate and complete microsatellite instability analysis in mismatch repair-deficient colorectal tumors. [electronic resource] by
- Agostini, Marco
- Enzo, Maria Vittoria
- Morandi, Luca
- Bedin, Chiara
- Pizzini, Silvia
- Mason, Silvia
- Bertorelle, Roberta
- Urso, Emanuele
- Mescoli, Claudia
- Lise, Mario
- Pucciarelli, Salvatore
- Nitti, Donato
Producer: 20100511
In:
Cancer biomarkers : section A of Disease markers vol. 6
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3374.
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3375.
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3376.
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Prospective evaluation of molecular screening for Lynch syndrome in patients with endometrial cancer ≤ 70 years. [electronic resource] by
- Leenen, Celine H M
- van Lier, Margot G F
- van Doorn, Helena C
- van Leerdam, Monique E
- Kooi, Sjarlot G
- de Waard, Judith
- Hoedemaeker, Robert F
- van den Ouweland, Ans M W
- Hulspas, Sanne M
- Dubbink, Hendrikus J
- Kuipers, Ernst J
- Wagner, Anja
- Dinjens, Winand N M
- Steyerberg, Ewout W
Producer: 20120606
In:
Gynecologic oncology vol. 125
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3377.
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First successful double-factor PGD for Lynch syndrome: monogenic analysis and comprehensive aneuploidy screening. [electronic resource] by
- Daina, G
- Ramos, L
- Obradors, A
- Rius, M
- Martinez-Pasarell, O
- Polo, A
- Del Rey, J
- Obradors, J
- Benet, J
- Navarro, J
Producer: 20131230
In:
Clinical genetics vol. 84
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3378.
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3379.
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Young age and a positive family history of colorectal cancer are complementary selection criteria for the identification of Lynch syndrome. [electronic resource] by
- Manders, P
- Spruijt, L
- Kets, C M
- Willems, H W
- Bodmer, D
- Hebeda, K M
- Nagtegaal, I D
- van Krieken, J H J M
- Ligtenberg, M J L
- Hoogerbrugge, N
Producer: 20111122
In:
European journal of cancer (Oxford, England : 1990) vol. 47
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3380.
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