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Msh2 deficiency leads to dysmyelination of the corpus callosum, impaired locomotion, and altered sensory function in mice. [electronic resource] by
- Diouf, Barthelemy
- Devaraju, Prakash
- Janke, Laura J
- Fan, Yiping
- Frase, Sharon
- Eddins, Donnie
- Peters, Jennifer L
- Kim, Jieun
- Pei, Deqing
- Cheng, Cheng
- Zakharenko, Stanislav S
- Evans, William E
Producer: 20180423
In:
Scientific reports vol. 6
Availability: No items available.
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Gene symbol: hMSH2. Disease: Hereditary nonpolyposis colorectal cancer. [electronic resource] by
- Sun, M H
- Cai, Qi
- Fu, Gang
- Ren, Shaungxi
- Mo, Shanjing
- Xu, Ye
- Ding, Chunwei
- Zhang, Taiming
- Zhu, Xiongzeng
- Xu, Xiaoli
- Min, Daliu
- Cai, Sanjun
- Luo, Dingcun
- Shi, Yingqiang
- Shi, Daren
Producer: 20040427
In:
Human genetics vol. 114
Availability: No items available.
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Founder effect of a pathogenic MSH2 mutation identified in Spanish families with Lynch syndrome. [electronic resource] by
- Menéndez, M
- Castellví-Bel, S
- Pineda, M
- de Cid, R
- Muñoz, J
- González, S
- Teulé, A
- Balaguer, F
- Ramón y Cajal, T
- Reñé, Josep M
- Blanco, I
- Castells, A
- Capellà, G
Producer: 20101207
In:
Clinical genetics vol. 78
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Medullary carcinoma of the pancreas in a man with hereditary nonpolyposis colorectal cancer due to a mutation of the MSH2 mismatch repair gene. [electronic resource] by
- Banville, Niamh
- Geraghty, Robert
- Fox, Edward
- Leahy, Dermot T
- Green, Andrew
- Keegan, Denise
- Geoghegan, Justin
- O'Donoghue, Diarmuid
- Hyland, John
- Sheahan, Kieran
Producer: 20061214
In:
Human pathology vol. 37
Availability: No items available.
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