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3621.
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3622.
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The p53 codon 72 variation is associated with the age of onset of hereditary non-polyposis colorectal cancer (HNPCC). [electronic resource] by
- Krüger, S
- Bier, A
- Engel, C
- Mangold, E
- Pagenstecher, C
- von Knebel Doeberitz, M
- Holinski-Feder, E
- Moeslein, G
- Schulmann, K
- Plaschke, J
- Rüschoff, J
- Schackert, H K
Producer: 20060724
In:
Journal of medical genetics vol. 42
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3623.
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3624.
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Refining the Amsterdam Criteria and Bethesda Guidelines: testing algorithms for the prediction of mismatch repair mutation status in the familial cancer clinic. [electronic resource] by
- Lipton, L R
- Johnson, V
- Cummings, C
- Fisher, S
- Risby, P
- Eftekhar Sadat, A T
- Cranston, T
- Izatt, L
- Sasieni, P
- Hodgson, S V
- Thomas, H J W
- Tomlinson, I P M
Producer: 20050118
In:
Journal of clinical oncology : official journal of the American Society of Clinical Oncology vol. 22
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3625.
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Genotype-phenotype comparison of German MLH1 and MSH2 mutation carriers clinically affected with Lynch syndrome: a report by the German HNPCC Consortium. [electronic resource] by
- Goecke, Timm
- Schulmann, Karsten
- Engel, Christoph
- Holinski-Feder, Elke
- Pagenstecher, Constanze
- Schackert, Hans K
- Kloor, Matthias
- Kunstmann, Erdmute
- Vogelsang, Holger
- Keller, Gisela
- Dietmaier, Wolfgang
- Mangold, Elisabeth
- Friedrichs, Nicolaus
- Propping, Peter
- Krüger, Stefan
- Gebert, Johannes
- Schmiegel, Wolff
- Rueschoff, Josef
- Loeffler, Markus
- Moeslein, Gabriela
Producer: 20060926
In:
Journal of clinical oncology : official journal of the American Society of Clinical Oncology vol. 24
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3626.
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3627.
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3628.
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Microsatellite instability and novel mismatch repair gene mutations in northern Chinese population with hereditary non-polyposis colorectal cancer. [electronic resource] by
- Sheng, Jian Qiu
- Chan, Tsun Leung
- Chan, Yee Wai
- Huang, Ji Sheng
- Chen, Ji Gui
- Zhang, Ming Zhi
- Guo, Xiu Lan
- Mu, Hong
- Chan, Annie Sy
- Li, Shi Rong
- Yuen, Siu Tsan
- Leung, Suet Yi
Producer: 20070105
In:
Chinese journal of digestive diseases vol. 7
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3629.
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Multifocal anaplastic astrocytoma in a patient with hereditary colorectal cancer, transcobalamin II deficiency, agenesis of the corpus callosum, mental retardation, and inherited PMS2 mutation. [electronic resource] by
- Gururangan, Sridharan
- Frankel, Wendy
- Broaddus, Russell
- Clendenning, Mark
- Senter, Leigha
- McDonald, Marie
- Eastwood, James
- Reardon, David
- Vredenburgh, James
- Quinn, Jennifer
- Friedman, Henry S
Producer: 20080521
In:
Neuro-oncology vol. 10
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3630.
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3631.
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3632.
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3633.
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Prevalence of MLH1 constitutional epimutations as a cause of Lynch syndrome in unselected versus selected consecutive series of patients with colorectal cancer. [electronic resource] by
- Castillejo, Adela
- Hernández-Illán, Eva
- Rodriguez-Soler, María
- Pérez-Carbonell, Lucía
- Egoavil, Cecilia
- Barberá, Victor M
- Castillejo, María-Isabel
- Guarinos, Carla
- Martínez-de-Dueñas, Eduardo
- Juan, María-Jose
- Sánchez-Heras, Ana-Beatriz
- García-Casado, Zaida
- Ruiz-Ponte, Clara
- Brea-Fernández, Alejandro
- Juárez, Miriam
- Bujanda, Luis
- Clofent, Juan
- Llor, Xavier
- Andreu, Montserrat
- Castells, Antoni
- Carracedo, Angel
- Alenda, Cristina
- Payá, Artemio
- Jover, Rodrigo
- Soto, José-Luis
Producer: 20160315
In:
Journal of medical genetics vol. 52
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3634.
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Population-based screening for Lynch syndrome in Western Australia. [electronic resource] by
- Schofield, Lyn
- Grieu, Fabienne
- Amanuel, Benhur
- Carrello, Amerigo
- Spagnolo, Dominic
- Kiraly, Cathy
- Pachter, Nicholas
- Goldblatt, Jack
- Platell, Cameron
- Levitt, Michael
- Stewart, Colin
- Salama, Paul
- Ee, Hooi
- Raftopoulous, Spiro
- Katris, Paul
- Threlfall, Tim
- Edkins, Edward
- Wallace, Marina
- Iacopetta, Barry
Producer: 20140813
In:
International journal of cancer vol. 135
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3635.
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3636.
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3637.
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High-sensitivity microsatellite instability assessment for the detection of mismatch repair defects in normal tissue of biallelic germline mismatch repair mutation carriers. [electronic resource] by
- González-Acosta, Maribel
- Marín, Fátima
- Puliafito, Benjamin
- Bonifaci, Nuria
- Fernández, Anna
- Navarro, Matilde
- Salvador, Hector
- Balaguer, Francesc
- Iglesias, Silvia
- Velasco, Angela
- Grau Garces, Elia
- Moreno, Victor
- Gonzalez-Granado, Luis Ignacio
- Guerra-García, Pilar
- Ayala, Rosa
- Florkin, Benoît
- Kratz, Christian
- Ripperger, Tim
- Rosenbaum, Thorsten
- Januszkiewicz-Lewandowska, Danuta
- Azizi, Amedeo A
- Ragab, Iman
- Nathrath, Michaela
- Pander, Hans-Jürgen
- Lobitz, Stephan
- Suerink, Manon
- Dahan, Karin
- Imschweiler, Thomas
- Demirsoy, Ugur
- Brunet, Joan
- Lázaro, Conxi
- Rueda, Daniel
- Wimmer, Katharina
- Capellá, Gabriel
- Pineda, Marta
Producer: 20210204
In:
Journal of medical genetics vol. 57
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3638.
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Associations of Pathogenic Variants in MLH1, MSH2, and MSH6 With Risk of Colorectal Adenomas and Tumors and With Somatic Mutations in Patients With Lynch Syndrome. [electronic resource] by
- Engel, Christoph
- Ahadova, Aysel
- Seppälä, Toni T
- Aretz, Stefan
- Bigirwamungu-Bargeman, Marloes
- Bläker, Hendrik
- Bucksch, Karolin
- Büttner, Reinhard
- de Vos Tot Nederveen Cappel, Wouter T
- Endris, Volker
- Holinski-Feder, Elke
- Holzapfel, Stefanie
- Hüneburg, Robert
- Jacobs, Maarten A J M
- Koornstra, Jan J
- Langers, Alexandra M
- Lepistö, Anna
- Morak, Monika
- Möslein, Gabriela
- Peltomäki, Päivi
- Pylvänäinen, Kirsi
- Rahner, Nils
- Renkonen-Sinisalo, Laura
- Schulmann, Karsten
- Steinke-Lange, Verena
- Stenzinger, Albrecht
- Strassburg, Christian P
- van de Meeberg, Paul C
- van Kouwen, Mariette
- van Leerdam, Monique
- Vangala, Deepak B
- Vecht, Juda
- Verhulst, Marie-Louise
- von Knebel Doeberitz, Magnus
- Weitz, Jürgen
- Zachariae, Silke
- Loeffler, Markus
- Mecklin, Jukka-Pekka
- Kloor, Matthias
- Vasen, Hans F
Producer: 20200710
In:
Gastroenterology vol. 158
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3639.
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3640.
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