000 | 01289 a2200397 4500 | ||
---|---|---|---|
005 | 20250511200538.0 | ||
264 | 0 | _c19911011 | |
008 | 199110s 0 0 eng d | ||
022 | _a0028-3878 | ||
024 | 7 |
_a10.1212/wnl.41.9.1513 _2doi |
|
040 |
_aNLM _beng _cNLM |
||
100 | 1 | _aTaylor, L D | |
245 | 0 | 0 |
_a9p monosomy in a patient with Gilles de la Tourette's syndrome. _h[electronic resource] |
260 |
_bNeurology _cSep 1991 |
||
300 |
_a1513-5 p. _bdigital |
||
500 | _aPublication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S. | ||
650 | 0 | 4 | _aAdolescent |
650 | 0 | 4 | _aChromosomes, Human, Pair 9 |
650 | 0 | 4 | _aDNA Probes |
650 | 0 | 4 | _aHumans |
650 | 0 | 4 |
_aInterferon Type I _xgenetics |
650 | 0 | 4 | _aKaryotyping |
650 | 0 | 4 | _aMale |
650 | 0 | 4 | _aMonosomy |
650 | 0 | 4 | _aPolymorphism, Restriction Fragment Length |
650 | 0 | 4 |
_aTourette Syndrome _xcomplications |
700 | 1 | _aKrizman, D B | |
700 | 1 | _aJankovic, J | |
700 | 1 | _aHayani, A | |
700 | 1 | _aSteuber, P C | |
700 | 1 | _aGreenberg, F | |
700 | 1 | _aFenwick, R G | |
700 | 1 | _aCaskey, C T | |
773 | 0 |
_tNeurology _gvol. 41 _gno. 9 _gp. 1513-5 |
|
856 | 4 | 0 |
_uhttps://doi.org/10.1212/wnl.41.9.1513 _zAvailable from publisher's website |
999 |
_c1686326 _d1686326 |