000 | 01024 a2200289 4500 | ||
---|---|---|---|
005 | 20250516033354.0 | ||
264 | 0 | _c20110623 | |
008 | 201106s 0 0 dan d | ||
022 | _a1603-6824 | ||
040 |
_aNLM _beng _cNLM |
||
100 | 1 | _aMøller, Rikke | |
245 | 0 | 0 |
_a[Submicroscopic chromosomal changes predispose to generalised epilepsy]. _h[electronic resource] |
260 |
_bUgeskrift for laeger _cApr 2011 |
||
300 |
_a1201-4 p. _bdigital |
||
500 | _aPublication Type: English Abstract; Journal Article | ||
650 | 0 | 4 | _aChromosome Deletion |
650 | 0 | 4 |
_aChromosomes, Human, Pair 1 _xgenetics |
650 | 0 | 4 |
_aChromosomes, Human, Pair 15 _xgenetics |
650 | 0 | 4 |
_aChromosomes, Human, Pair 16 _xgenetics |
650 | 0 | 4 |
_aChromosomes, Human, Pair 22 _xgenetics |
650 | 0 | 4 |
_aEpilepsy, Generalized _xgenetics |
650 | 0 | 4 | _aGenetic Predisposition to Disease |
650 | 0 | 4 | _aHumans |
650 | 0 | 4 |
_aMeiosis _xgenetics |
700 | 1 | _aHjalgrim, Helle | |
773 | 0 |
_tUgeskrift for laeger _gvol. 173 _gno. 16-17 _gp. 1201-4 |
|
999 |
_c20767366 _d20767366 |