| 000 | 01751 a2200541 4500 | ||
|---|---|---|---|
| 005 | 20250515094914.0 | ||
| 264 | 0 | _c20080501 | |
| 008 | 200805s 0 0 eng d | ||
| 022 | _a1538-7836 | ||
| 024 | 7 |
_a10.1111/j.1538-7836.2008.02849.x _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aTai, S J | |
| 245 | 0 | 0 |
_aA viable mouse model of factor X deficiency provides evidence for maternal transfer of factor X. _h[electronic resource] |
| 260 |
_bJournal of thrombosis and haemostasis : JTH _c02 2008 |
||
| 300 |
_a339-45 p. _bdigital |
||
| 500 | _aPublication Type: Journal Article; Research Support, N.I.H., Extramural | ||
| 650 | 0 | 4 | _aAmino Acid Substitution |
| 650 | 0 | 4 | _aAnimals |
| 650 | 0 | 4 |
_aCardiomyopathies _xetiology |
| 650 | 0 | 4 |
_aExons _xgenetics |
| 650 | 0 | 4 |
_aFactor X _xgenetics |
| 650 | 0 | 4 |
_aFactor X Deficiency _xcomplications |
| 650 | 0 | 4 | _aFemale |
| 650 | 0 | 4 |
_aFetal Death _xgenetics |
| 650 | 0 | 4 | _aFibrosis |
| 650 | 0 | 4 |
_aGene Targeting _xmethods |
| 650 | 0 | 4 | _aGenes, Lethal |
| 650 | 0 | 4 | _aGenetic Complementation Test |
| 650 | 0 | 4 |
_aGenomic Imprinting _xgenetics |
| 650 | 0 | 4 | _aGenotype |
| 650 | 0 | 4 |
_aHemosiderosis _xetiology |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 | _aMale |
| 650 | 0 | 4 | _aMice |
| 650 | 0 | 4 | _aMice, Knockout |
| 650 | 0 | 4 |
_aMice, Transgenic _xblood |
| 650 | 0 | 4 | _aModels, Animal |
| 650 | 0 | 4 |
_aMyocardium _xpathology |
| 700 | 1 | _aHerzog, R W | |
| 700 | 1 | _aMargaritis, P | |
| 700 | 1 | _aArruda, V R | |
| 700 | 1 | _aChu, K | |
| 700 | 1 | _aGolden, J A | |
| 700 | 1 | _aLabosky, P A | |
| 700 | 1 | _aHigh, K A | |
| 773 | 0 |
_tJournal of thrombosis and haemostasis : JTH _gvol. 6 _gno. 2 _gp. 339-45 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1111/j.1538-7836.2008.02849.x _zAvailable from publisher's website |
| 999 |
_c17551608 _d17551608 |
||