| 000 | 01202 a2200349 4500 | ||
|---|---|---|---|
| 005 | 20250517121530.0 | ||
| 264 | 0 | _c20170522 | |
| 008 | 201705s 0 0 eng d | ||
| 022 | _a1471-499X | ||
| 024 | 7 |
_a10.1016/j.molmed.2016.09.007 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aShirts, Brian H | |
| 245 | 0 | 0 |
_aFamily-Specific Variants and the Limits of Human Genetics. _h[electronic resource] |
| 260 |
_bTrends in molecular medicine _cNov 2016 |
||
| 300 |
_a925-934 p. _bdigital |
||
| 500 | _aPublication Type: Journal Article; Review | ||
| 650 | 0 | 4 |
_aGenetic Predisposition to Disease _xgenetics |
| 650 | 0 | 4 |
_aGenetic Testing _xmethods |
| 650 | 0 | 4 | _aGenetic Variation |
| 650 | 0 | 4 |
_aGenetics, Medical _xmethods |
| 650 | 0 | 4 | _aGenotype |
| 650 | 0 | 4 |
_aHigh-Throughput Nucleotide Sequencing _xmethods |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 | _aPedigree |
| 650 | 0 | 4 | _aPhenotype |
| 650 | 0 | 4 | _aPolymorphism, Single Nucleotide |
| 650 | 0 | 4 | _aUncertainty |
| 700 | 1 | _aPritchard, Colin C | |
| 700 | 1 | _aWalsh, Tom | |
| 773 | 0 |
_tTrends in molecular medicine _gvol. 22 _gno. 11 _gp. 925-934 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1016/j.molmed.2016.09.007 _zAvailable from publisher's website |
| 999 |
_c26516773 _d26516773 |
||