| 000 | 01840 a2200493 4500 | ||
|---|---|---|---|
| 005 | 20250516151754.0 | ||
| 264 | 0 | _c20130806 | |
| 008 | 201308s 0 0 eng d | ||
| 022 | _a1091-6490 | ||
| 024 | 7 |
_a10.1073/pnas.1220537110 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aDrost, Mark | |
| 245 | 0 | 0 |
_aGenetic screens to identify pathogenic gene variants in the common cancer predisposition Lynch syndrome. _h[electronic resource] |
| 260 |
_bProceedings of the National Academy of Sciences of the United States of America _cJun 2013 |
||
| 300 |
_a9403-8 p. _bdigital |
||
| 500 | _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't | ||
| 650 | 0 | 4 |
_aAmino Acid Substitution _xgenetics |
| 650 | 0 | 4 | _aBase Sequence |
| 650 | 0 | 4 |
_aColorectal Neoplasms, Hereditary Nonpolyposis _xgenetics |
| 650 | 0 | 4 |
_aGenetic Predisposition to Disease _xgenetics |
| 650 | 0 | 4 | _aGenetic Testing |
| 650 | 0 | 4 | _aGenetic Variation |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 |
_aMicrosatellite Repeats _xgenetics |
| 650 | 0 | 4 | _aModels, Molecular |
| 650 | 0 | 4 | _aMolecular Sequence Data |
| 650 | 0 | 4 |
_aMutS Homolog 2 Protein _xchemistry |
| 650 | 0 | 4 | _aMutagenesis |
| 650 | 0 | 4 |
_aMutation _xgenetics |
| 650 | 0 | 4 |
_aReverse Genetics _xmethods |
| 650 | 0 | 4 | _aSequence Analysis, DNA |
| 650 | 0 | 4 | _aThioguanine |
| 650 | 0 | 4 |
_aVirulence _xgenetics |
| 700 | 1 | _aLützen, Anne | |
| 700 | 1 | _avan Hees, Sandrine | |
| 700 | 1 | _aFerreira, Daniel | |
| 700 | 1 | _aCalléja, Fabienne | |
| 700 | 1 | _aZonneveld, José B M | |
| 700 | 1 | _aNielsen, Finn Cilius | |
| 700 | 1 | _aRasmussen, Lene Juel | |
| 700 | 1 | _ade Wind, Niels | |
| 773 | 0 |
_tProceedings of the National Academy of Sciences of the United States of America _gvol. 110 _gno. 23 _gp. 9403-8 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1073/pnas.1220537110 _zAvailable from publisher's website |
| 999 |
_c22767224 _d22767224 |
||