000 01540 a2200505 4500
005 20250516050539.0
264 0 _c20120531
008 201205s 0 0 eng d
022 _a1098-1004
024 7 _a10.1002/humu.21570
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aAvila, M
245 0 0 _aGLI3 is rarely implicated in OFD syndromes with midline abnormalities.
_h[electronic resource]
260 _bHuman mutation
_cNov 2011
300 _a1332-3 p.
_bdigital
500 _aPublication Type: Letter; Research Support, Non-U.S. Gov't; Comment
650 0 4 _aAbnormalities, Multiple
_xgenetics
650 0 4 _aHumans
650 0 4 _aKruppel-Like Transcription Factors
_xgenetics
650 0 4 _aMutation
650 0 4 _aNerve Tissue Proteins
_xgenetics
650 0 4 _aPallister-Hall Syndrome
_xpathology
650 0 4 _aPolydactyly
_xpathology
650 0 4 _aSyndactyly
_xpathology
700 1 _aGigot, N
700 1 _aAral, B
700 1 _aCallier, P
700 1 _aGautier, E
700 1 _aThevenon, J
700 1 _aPasquier, L
700 1 _aLopez, E
700 1 _aGueneau, L
700 1 _aDuplomb, L
700 1 _aGoldenberg, A
700 1 _aBaumann, C
700 1 _aCormier, V
700 1 _aMarlin, S
700 1 _aMasurel-Paulet, A
700 1 _aHuet, F
700 1 _aAttiƩ-Bitach, T
700 1 _aFaivre, L
700 1 _aThauvin-Robinet, C
773 0 _tHuman mutation
_gvol. 32
_gno. 11
_gp. 1332-3
856 4 0 _uhttps://doi.org/10.1002/humu.21570
_zAvailable from publisher's website
999 _c21042693
_d21042693