Results
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3261.
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Recurrence and variability of germline EPCAM deletions in Lynch syndrome. [electronic resource] by
- Kuiper, Roland P
- Vissers, Lisenka E L M
- Venkatachalam, Ramprasath
- Bodmer, Danielle
- Hoenselaar, Eveline
- Goossens, Monique
- Haufe, Aline
- Kamping, Eveline
- Niessen, Renée C
- Hogervorst, Frans B L
- Gille, Johan J P
- Redeker, Bert
- Tops, Carli M J
- van Gijn, Marielle E
- van den Ouweland, Ans M W
- Rahner, Nils
- Steinke, Verena
- Kahl, Philip
- Holinski-Feder, Elke
- Morak, Monika
- Kloor, Matthias
- Stemmler, Susanne
- Betz, Beate
- Hutter, Pierre
- Bunyan, David J
- Syngal, Sapna
- Culver, Julie O
- Graham, Tracy
- Chan, Tsun L
- Nagtegaal, Iris D
- van Krieken, J Han J M
- Schackert, Hans K
- Hoogerbrugge, Nicoline
- van Kessel, Ad Geurts
- Ligtenberg, Marjolijn J L
Producer: 20110722
In:
Human mutation vol. 32
Availability: No items available.
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3262.
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3263.
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3264.
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Clinicopathological features of breast cancer in Japanese female patients with Lynch syndrome. [electronic resource] by
- Kanaya, Nobuhiko
- Tanakaya, Kohji
- Yamasaki, Rie
- Arata, Takashi
- Shigeyasu, Kunitoshi
- Aoki, Hideki
- Morito, Toshiaki
- Sanaii, Hiromi
- Akagi, Kiwamu
- Fujiwara, Toshiyoshi
Producer: 20190906
In:
Breast cancer (Tokyo, Japan) vol. 26
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3265.
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3266.
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Seven new mutations in hMSH2, an HNPCC gene, identified by denaturing gradient-gel electrophoresis. [electronic resource] by
- Wijnen, J
- Vasen, H
- Khan, P M
- Menko, F H
- van der Klift, H
- van Leeuwen, C
- van den Broek, M
- van Leeuwen-Cornelisse, I
- Nagengast, F
- Meijers-Heijboer, A
Producer: 19950524
In:
American journal of human genetics vol. 56
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3267.
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3268.
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3269.
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3270.
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3271.
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3272.
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3273.
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Low levels of microsatellite instability characterize MLH1 and MSH2 HNPCC carriers before tumor diagnosis. [electronic resource] by
- Alazzouzi, Hafid
- Domingo, Enric
- González, Sara
- Blanco, Ignacio
- Armengol, Manel
- Espín, Eloi
- Plaja, Alberto
- Schwartz, Simó
- Capella, Gabriel
- Schwartz, Simó
Producer: 20050517
In:
Human molecular genetics vol. 14
Availability: No items available.
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3274.
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3275.
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Aetiology of colorectal cancer and relevance of monogenic inheritance. [electronic resource] by
- Ponz de Leon, M
- Benatti, P
- Borghi, F
- Pedroni, M
- Scarselli, A
- Di Gregorio, C
- Losi, L
- Viel, A
- Genuardi, M
- Abbati, G
- Rossi, G
- Menigatti, M
- Lamberti, I
- Ponti, G
- Roncucci, L
Producer: 20040226
In:
Gut vol. 53
Availability: No items available.
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3276.
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3277.
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3278.
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3279.
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A frame-shift mutation of PMS2 is a widespread cause of Lynch syndrome. [electronic resource] by
- Clendenning, M
- Senter, L
- Hampel, H
- Robinson, K Lagerstedt
- Sun, S
- Buchanan, D
- Walsh, M D
- Nilbert, M
- Green, J
- Potter, J
- Lindblom, A
- de la Chapelle, A
Producer: 20080811
In:
Journal of medical genetics vol. 45
Availability: No items available.
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3280.
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