| 000 | 01876 a2200613 4500 | ||
|---|---|---|---|
| 005 | 20250513195603.0 | ||
| 264 | 0 | _c20000127 | |
| 008 | 200001s 0 0 eng d | ||
| 022 | _a0002-9297 | ||
| 024 | 7 |
_a10.1086/302649 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aXiong, L | |
| 245 | 0 | 0 |
_aMapping of a gene determining familial partial epilepsy with variable foci to chromosome 22q11-q12. _h[electronic resource] |
| 260 |
_bAmerican journal of human genetics _cDec 1999 |
||
| 300 |
_a1698-710 p. _bdigital |
||
| 500 | _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't | ||
| 650 | 0 | 4 | _aAustralia |
| 650 | 0 | 4 | _aCanada |
| 650 | 0 | 4 | _aChromosome Mapping |
| 650 | 0 | 4 |
_aChromosomes, Human, Pair 22 _xgenetics |
| 650 | 0 | 4 |
_aEpilepsies, Partial _xgenetics |
| 650 | 0 | 4 | _aFemale |
| 650 | 0 | 4 | _aFounder Effect |
| 650 | 0 | 4 |
_aGenes, Dominant _xgenetics |
| 650 | 0 | 4 | _aGenetic Heterogeneity |
| 650 | 0 | 4 |
_aGenetic Linkage _xgenetics |
| 650 | 0 | 4 | _aGenetic Markers |
| 650 | 0 | 4 |
_aHaplotypes _xgenetics |
| 650 | 0 | 4 | _aHomozygote |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 | _aMale |
| 650 | 0 | 4 | _aPedigree |
| 650 | 0 | 4 | _aPenetrance |
| 650 | 0 | 4 |
_aPolymorphism, Genetic _xgenetics |
| 650 | 0 | 4 |
_aReceptors, Purinergic P1 _xgenetics |
| 650 | 0 | 4 |
_aRecombination, Genetic _xgenetics |
| 700 | 1 | _aLabuda, M | |
| 700 | 1 | _aLi, D S | |
| 700 | 1 | _aHudson, T J | |
| 700 | 1 | _aDesbiens, R | |
| 700 | 1 | _aPatry, G | |
| 700 | 1 | _aVerret, S | |
| 700 | 1 | _aLangevin, P | |
| 700 | 1 | _aMercho, S | |
| 700 | 1 | _aSeni, M H | |
| 700 | 1 | _aScheffer, I | |
| 700 | 1 | _aDubeau, F | |
| 700 | 1 | _aBerkovic, S F | |
| 700 | 1 | _aAndermann, F | |
| 700 | 1 | _aAndermann, E | |
| 700 | 1 | _aPandolfo, M | |
| 773 | 0 |
_tAmerican journal of human genetics _gvol. 65 _gno. 6 _gp. 1698-710 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1086/302649 _zAvailable from publisher's website |
| 999 |
_c10534155 _d10534155 |
||