000 01503 a2200481 4500
005 20250515235240.0
264 0 _c20110329
008 201103s 0 0 eng d
022 _a1525-5069
024 7 _a10.1016/j.yebeh.2010.07.007
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aVendrame, Martina
245 0 0 _aEpilepsy in Prader-Willi syndrome: clinical characteristics and correlation to genotype.
_h[electronic resource]
260 _bEpilepsy & behavior : E&B
_cNov 2010
300 _a306-10 p.
_bdigital
500 _aPublication Type: Journal Article
650 0 4 _aAdolescent
650 0 4 _aChild
650 0 4 _aChild, Preschool
650 0 4 _aChromosome Deletion
650 0 4 _aElectroencephalography
650 0 4 _aEpilepsy
_xclassification
650 0 4 _aFemale
650 0 4 _aGenomic Imprinting
650 0 4 _aGenotype
650 0 4 _aHumans
650 0 4 _aInfant
650 0 4 _aMale
650 0 4 _aMutation
650 0 4 _aPrader-Willi Syndrome
_xcomplications
650 0 4 _aRetrospective Studies
650 0 4 _aRisk Factors
650 0 4 _aStatistics as Topic
650 0 4 _aYoung Adult
700 1 _aMaski, Kiran P
700 1 _aChatterjee, Madhumouli
700 1 _aHeshmati, Arezou
700 1 _aKrishnamoorthy, Kalpathy
700 1 _aTan, Wen-Hann
700 1 _aKothare, Sanjeev V
773 0 _tEpilepsy & behavior : E&B
_gvol. 19
_gno. 3
_gp. 306-10
856 4 0 _uhttps://doi.org/10.1016/j.yebeh.2010.07.007
_zAvailable from publisher's website
999 _c20063355
_d20063355