| 000 | 01887 a2200589 4500 | ||
|---|---|---|---|
| 005 | 20250513220102.0 | ||
| 264 | 0 | _c20001121 | |
| 008 | 200011s 0 0 eng d | ||
| 022 | _a0964-6906 | ||
| 024 | 7 |
_a10.1093/hmg/9.14.2067 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aGeurts, J M | |
| 245 | 0 | 0 |
_aIdentification of TNFRSF1B as a novel modifier gene in familial combined hyperlipidemia. _h[electronic resource] |
| 260 |
_bHuman molecular genetics _cSep 2000 |
||
| 300 |
_a2067-74 p. _bdigital |
||
| 500 | _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S. | ||
| 650 | 0 | 4 | _aAdult |
| 650 | 0 | 4 | _aAlleles |
| 650 | 0 | 4 |
_aApolipoproteins B _xbiosynthesis |
| 650 | 0 | 4 | _aCase-Control Studies |
| 650 | 0 | 4 | _aChromosomes, Human, Pair 1 |
| 650 | 0 | 4 | _aDNA Mutational Analysis |
| 650 | 0 | 4 | _aExons |
| 650 | 0 | 4 | _aFamily Health |
| 650 | 0 | 4 | _aFemale |
| 650 | 0 | 4 | _aGenetic Linkage |
| 650 | 0 | 4 | _aGenotype |
| 650 | 0 | 4 | _aHaplotypes |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 |
_aHyperlipidemia, Familial Combined _xblood |
| 650 | 0 | 4 | _aIntrons |
| 650 | 0 | 4 | _aLinear Models |
| 650 | 0 | 4 | _aLinkage Disequilibrium |
| 650 | 0 | 4 | _aMale |
| 650 | 0 | 4 | _aMiddle Aged |
| 650 | 0 | 4 | _aPhenotype |
| 650 | 0 | 4 | _aPolymorphism, Single Nucleotide |
| 650 | 0 | 4 |
_aReceptors, Tumor Necrosis Factor _xblood |
| 650 | 0 | 4 | _aReceptors, Tumor Necrosis Factor, Type II |
| 650 | 0 | 4 | _aTumor Necrosis Factor-alpha |
| 700 | 1 | _aJanssen, R G | |
| 700 | 1 | _avan Greevenbroek, M M | |
| 700 | 1 | _avan der Kallen, C J | |
| 700 | 1 | _aCantor, R M | |
| 700 | 1 | _aBu, X | |
| 700 | 1 | _aAouizerat, B E | |
| 700 | 1 | _aAllayee, H | |
| 700 | 1 | _aRotter, J I | |
| 700 | 1 | _ade Bruin, T W | |
| 773 | 0 |
_tHuman molecular genetics _gvol. 9 _gno. 14 _gp. 2067-74 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1093/hmg/9.14.2067 _zAvailable from publisher's website |
| 999 |
_c10906232 _d10906232 |
||