000 01069 a2200337 4500
005 20250513094018.0
264 0 _c19960925
008 199609s 0 0 eng d
022 _a0022-2593
024 7 _a10.1136/jmg.33.4.319
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aPilz, D T
245 0 0 _aSyndromes with lissencephaly.
_h[electronic resource]
260 _bJournal of medical genetics
_cApr 1996
300 _a319-23 p.
_bdigital
500 _aPublication Type: Journal Article; Review
650 0 4 _aBrain
_xabnormalities
650 0 4 _aCell Movement
650 0 4 _aChild
650 0 4 _aGenetic Counseling
650 0 4 _aHumans
650 0 4 _aIntellectual Disability
_xgenetics
650 0 4 _aNeurons
_xcytology
650 0 4 _aRadionuclide Imaging
650 0 4 _aSeizures
_xcongenital
650 0 4 _aSyndrome
650 0 4 _aTomography, X-Ray Computed
700 1 _aQuarrell, O W
773 0 _tJournal of medical genetics
_gvol. 33
_gno. 4
_gp. 319-23
856 4 0 _uhttps://doi.org/10.1136/jmg.33.4.319
_zAvailable from publisher's website
999 _c8727369
_d8727369