| 000 | 01638 a2200505 4500 | ||
|---|---|---|---|
| 005 | 20250513151157.0 | ||
| 264 | 0 | _c19980910 | |
| 008 | 199809s 0 0 eng d | ||
| 022 | _a1079-5642 | ||
| 024 | 7 |
_a10.1161/01.atv.18.8.1287 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aKyrle, P A | |
| 245 | 0 | 0 |
_aClinical studies and thrombin generation in patients homozygous or heterozygous for the G20210A mutation in the prothrombin gene. _h[electronic resource] |
| 260 |
_bArteriosclerosis, thrombosis, and vascular biology _cAug 1998 |
||
| 300 |
_a1287-91 p. _bdigital |
||
| 500 | _aPublication Type: Clinical Trial; Journal Article; Multicenter Study; Research Support, Non-U.S. Gov't | ||
| 650 | 0 | 4 | _aAdult |
| 650 | 0 | 4 | _aAlleles |
| 650 | 0 | 4 |
_aDNA _xblood |
| 650 | 0 | 4 | _aFemale |
| 650 | 0 | 4 | _aGenetic Carrier Screening |
| 650 | 0 | 4 | _aHeterozygote |
| 650 | 0 | 4 | _aHomozygote |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 | _aMale |
| 650 | 0 | 4 | _aMiddle Aged |
| 650 | 0 | 4 |
_aMutation _xgenetics |
| 650 | 0 | 4 | _aProspective Studies |
| 650 | 0 | 4 |
_aProthrombin _xanalysis |
| 650 | 0 | 4 |
_aThrombin _xanalysis |
| 650 | 0 | 4 |
_aThrombophilia _xblood |
| 700 | 1 | _aMannhalter, C | |
| 700 | 1 | _aBéguin, S | |
| 700 | 1 | _aStümpflen, A | |
| 700 | 1 | _aHirschl, M | |
| 700 | 1 | _aWeltermann, A | |
| 700 | 1 | _aStain, M | |
| 700 | 1 | _aBrenner, B | |
| 700 | 1 | _aSpeiser, W | |
| 700 | 1 | _aPabinger, I | |
| 700 | 1 | _aLechner, K | |
| 700 | 1 | _aEichinger, S | |
| 773 | 0 |
_tArteriosclerosis, thrombosis, and vascular biology _gvol. 18 _gno. 8 _gp. 1287-91 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1161/01.atv.18.8.1287 _zAvailable from publisher's website |
| 999 |
_c9679641 _d9679641 |
||