000 02165 a2200745 4500
005 20250515063511.0
264 0 _c20070501
008 200705s 0 0 eng d
022 _a1526-632X
024 7 _a10.1212/01.wnl.0000259086.34769.78
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aTemudo, T
245 0 0 _aStereotypies in Rett syndrome: analysis of 83 patients with and without detected MECP2 mutations.
_h[electronic resource]
260 _bNeurology
_cApr 2007
300 _a1183-7 p.
_bdigital
500 _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't
650 0 4 _aAdolescent
650 0 4 _aAdult
650 0 4 _aChild
650 0 4 _aChild, Preschool
650 0 4 _aComorbidity
650 0 4 _aDNA Mutational Analysis
_xmethods
650 0 4 _aFemale
650 0 4 _aGenetic Predisposition to Disease
_xepidemiology
650 0 4 _aGenetic Testing
_xmethods
650 0 4 _aHeterozygote
650 0 4 _aHumans
650 0 4 _aIncidence
650 0 4 _aInfant
650 0 4 _aMale
650 0 4 _aMethyl-CpG-Binding Protein 2
_xgenetics
650 0 4 _aMutation
650 0 4 _aPolymorphism, Single Nucleotide
_xgenetics
650 0 4 _aPortugal
_xepidemiology
650 0 4 _aPrevalence
650 0 4 _aRett Syndrome
_xgenetics
650 0 4 _aRisk Assessment
_xmethods
650 0 4 _aRisk Factors
650 0 4 _aStereotypic Movement Disorder
_xepidemiology
700 1 _aOliveira, P
700 1 _aSantos, M
700 1 _aDias, K
700 1 _aVieira, J
700 1 _aMoreira, A
700 1 _aCalado, E
700 1 _aCarrilho, I
700 1 _aOliveira, G
700 1 _aLevy, A
700 1 _aBarbot, C
700 1 _aFonseca, M
700 1 _aCabral, A
700 1 _aDias, A
700 1 _aCabral, P
700 1 _aMonteiro, J
700 1 _aBorges, L
700 1 _aGomes, R
700 1 _aBarbosa, C
700 1 _aMira, G
700 1 _aEusébio, F
700 1 _aSantos, M
700 1 _aSequeiros, J
700 1 _aMaciel, P
773 0 _tNeurology
_gvol. 68
_gno. 15
_gp. 1183-7
856 4 0 _uhttps://doi.org/10.1212/01.wnl.0000259086.34769.78
_zAvailable from publisher's website
999 _c16971481
_d16971481