000 01102 a2200349 4500
005 20250513034310.0
264 0 _c19950831
008 199508s 0 0 eng d
022 _a1350-7540
024 7 _a10.1097/00019052-199504000-00013
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aPercy, A K
245 0 0 _aRett syndrome.
_h[electronic resource]
260 _bCurrent opinion in neurology
_cApr 1995
300 _a156-60 p.
_bdigital
500 _aPublication Type: Journal Article; Review
650 0 4 _aBrain
_xpathology
650 0 4 _aChild
650 0 4 _aChild, Preschool
650 0 4 _aChromosomes, Human, Pair 3
650 0 4 _aDiagnosis, Differential
650 0 4 _aDiagnostic Imaging
650 0 4 _aFemale
650 0 4 _aHumans
650 0 4 _aInfant
650 0 4 _aInfant, Newborn
650 0 4 _aRett Syndrome
_xgenetics
650 0 4 _aTranslocation, Genetic
_xgenetics
650 0 4 _aX Chromosome
773 0 _tCurrent opinion in neurology
_gvol. 8
_gno. 2
_gp. 156-60
856 4 0 _uhttps://doi.org/10.1097/00019052-199504000-00013
_zAvailable from publisher's website
999 _c7620028
_d7620028