The founder mutation MSH2*1906G-->C is an important cause of hereditary nonpolyposis colorectal cancer in the Ashkenazi Jewish population (Q34161196)
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| Language | Label | Description | Also known as |
|---|---|---|---|
| English | The founder mutation MSH2*1906G-->C is an important cause of hereditary nonpolyposis colorectal cancer in the Ashkenazi Jewish population |
scientific article |
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The founder mutation MSH2*1906G-->C is an important cause of hereditary nonpolyposis colorectal cancer in the Ashkenazi Jewish population (English)
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J N Weitzel
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W D Foulkes
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G Rennert
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K Offit
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B Bressac-De Paillerets
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A De La Chapelle
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I Thiffault
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S B Gruber
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N Hamel
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C Lee
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A Markowitz
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A Figer
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E Friedman
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D Farber
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C M T Greenwood
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J D Bonner
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K Nafa
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V Marcus
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L Tomsho
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J Gebert
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F A Macrae
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C L Gaff
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P K Gregersen
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P H Gordon
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E MacNamara
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M-C King
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H Hampel
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J Boyd
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G Chong
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N A Ellis
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26 November 2002
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71
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1395-1412
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