000 01481 a2200433 4500
005 20250515032635.0
264 0 _c20060927
008 200609s 0 0 eng d
022 _a0887-8994
024 7 _a10.1016/j.pediatrneurol.2005.12.001
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aElias, Renata C
245 0 0 _aDeletion of 17p13 and LIS1 gene mutation in isolated lissencephaly sequence.
_h[electronic resource]
260 _bPediatric neurology
_cJul 2006
300 _a42-6 p.
_bdigital
500 _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't
650 0 4 _a1-Alkyl-2-acetylglycerophosphocholine Esterase
650 0 4 _aBase Sequence
650 0 4 _aBrain
_xabnormalities
650 0 4 _aChild, Preschool
650 0 4 _aChromosomes, Human, Pair 17
_xgenetics
650 0 4 _aFemale
650 0 4 _aGene Deletion
650 0 4 _aHumans
650 0 4 _aInfant
650 0 4 _aMale
650 0 4 _aMicrotubule-Associated Proteins
_xgenetics
650 0 4 _aPolymorphism, Single-Stranded Conformational
700 1 _aGalera, Marcial F
700 1 _aSchnabel, Beatriz
700 1 _aBriones, Marcelo R S
700 1 _aBorri, Maria L
700 1 _aLipay, Monica
700 1 _aCarvalheira, Gianna
700 1 _aBrunoni, Decio
700 1 _aMelaragno, Maria I
773 0 _tPediatric neurology
_gvol. 35
_gno. 1
_gp. 42-6
856 4 0 _uhttps://doi.org/10.1016/j.pediatrneurol.2005.12.001
_zAvailable from publisher's website
999 _c16406606
_d16406606