000 01319 a2200385 4500
005 20250514024824.0
264 0 _c20020318
008 200203s 0 0 eng d
022 _a0013-9580
024 7 _a10.1046/j.1528-1157.2001.29700.x
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aGarcía, D M
245 0 0 _aRing 20 chromosome syndrome with epilepsy and dysmorphic features: a case report.
_h[electronic resource]
260 _bEpilepsia
_cDec 2001
300 _a1607-10 p.
_bdigital
500 _aPublication Type: Case Reports; Journal Article
650 0 4 _aAbnormalities, Multiple
_xdiagnosis
650 0 4 _aChild, Preschool
650 0 4 _aChromosomes, Human, Pair 20
_xgenetics
650 0 4 _aCytogenetic Analysis
650 0 4 _aElectroencephalography
_xstatistics & numerical data
650 0 4 _aEpilepsy
_xdiagnosis
650 0 4 _aEvoked Potentials, Auditory, Brain Stem
_xphysiology
650 0 4 _aHumans
650 0 4 _aKaryotyping
650 0 4 _aMagnetic Resonance Imaging
650 0 4 _aMale
650 0 4 _aRing Chromosomes
650 0 4 _aSyndrome
700 1 _aOrtiz, R
700 1 _aGómez, A
700 1 _aBarriuso, E
773 0 _tEpilepsia
_gvol. 42
_gno. 12
_gp. 1607-10
856 4 0 _uhttps://doi.org/10.1046/j.1528-1157.2001.29700.x
_zAvailable from publisher's website
999 _c11786426
_d11786426