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