| 000 | 01019 a2200313 4500 | ||
|---|---|---|---|
| 005 | 20250513095938.0 | ||
| 264 | 0 | _c19961018 | |
| 008 | 199610s 0 0 eng d | ||
| 022 | _a0741-0395 | ||
| 024 | 7 |
_a10.1002/gepi.1370120621 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aMitchell, L E | |
| 245 | 0 | 0 |
_aSequential analysis of marker data for a rare oligogenic disease. _h[electronic resource] |
| 260 |
_bGenetic epidemiology _c1995 |
||
| 300 |
_a647-51 p. _bdigital |
||
| 500 | _aPublication Type: Journal Article | ||
| 650 | 0 | 4 | _aFemale |
| 650 | 0 | 4 |
_aGenetic Diseases, Inborn _xgenetics |
| 650 | 0 | 4 | _aGenetic Markers |
| 650 | 0 | 4 | _aGenetic Predisposition to Disease |
| 650 | 0 | 4 | _aGenetics, Population |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 | _aLinkage Disequilibrium |
| 650 | 0 | 4 | _aLod Score |
| 650 | 0 | 4 | _aMale |
| 650 | 0 | 4 | _aNuclear Family |
| 773 | 0 |
_tGenetic epidemiology _gvol. 12 _gno. 6 _gp. 647-51 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1002/gepi.1370120621 _zAvailable from publisher's website |
| 999 |
_c8784552 _d8784552 |
||