| 000 | 01504 a2200445 4500 | ||
|---|---|---|---|
| 005 | 20250514195825.0 | ||
| 264 | 0 | _c20050425 | |
| 008 | 200504s 0 0 eng d | ||
| 022 | _a0964-6906 | ||
| 024 | 7 |
_a10.1093/hmg/ddh270 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aFreedman, Matthew L | |
| 245 | 0 | 0 |
_aCommon variation in BRCA2 and breast cancer risk: a haplotype-based analysis in the Multiethnic Cohort. _h[electronic resource] |
| 260 |
_bHuman molecular genetics _cOct 2004 |
||
| 300 |
_a2431-41 p. _bdigital |
||
| 500 | _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't | ||
| 650 | 0 | 4 | _aAged |
| 650 | 0 | 4 |
_aBreast Neoplasms _xethnology |
| 650 | 0 | 4 | _aCase-Control Studies |
| 650 | 0 | 4 | _aCohort Studies |
| 650 | 0 | 4 | _aFemale |
| 650 | 0 | 4 | _aGenes, BRCA2 |
| 650 | 0 | 4 |
_aGenetic Predisposition to Disease _xgenetics |
| 650 | 0 | 4 |
_aHaplotypes _xgenetics |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 | _aMiddle Aged |
| 650 | 0 | 4 |
_aMutation, Missense _xgenetics |
| 650 | 0 | 4 | _aPolymorphism, Single Nucleotide |
| 650 | 0 | 4 | _aRisk Factors |
| 700 | 1 | _aPenney, Kathryn L | |
| 700 | 1 | _aStram, Daniel O | |
| 700 | 1 | _aLe Marchand, Loïc | |
| 700 | 1 | _aHirschhorn, Joel N | |
| 700 | 1 | _aKolonel, Laurence N | |
| 700 | 1 | _aAltshuler, David | |
| 700 | 1 | _aHenderson, Brian E | |
| 700 | 1 | _aHaiman, Christopher A | |
| 773 | 0 |
_tHuman molecular genetics _gvol. 13 _gno. 20 _gp. 2431-41 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1093/hmg/ddh270 _zAvailable from publisher's website |
| 999 |
_c15016456 _d15016456 |
||