000 01633 a2200457 4500
005 20250515033138.0
264 0 _c20060928
008 200609s 0 0 eng d
022 _a1769-7212
024 7 _a10.1016/j.ejmg.2005.10.133
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aSchwarzbraun, Thomas
245 0 0 _aGenomic analysis of five chromosome 7p deletion patients with Greig cephalopolysyndactyly syndrome (GCPS).
_h[electronic resource]
260 _bEuropean journal of medical genetics
_c
300 _a338-45 p.
_bdigital
500 _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't
650 0 4 _aAbnormalities, Multiple
_xgenetics
650 0 4 _aChromosome Deletion
650 0 4 _aChromosomes, Human, Pair 7
650 0 4 _aCraniofacial Abnormalities
_xgenetics
650 0 4 _aGenetic Techniques
650 0 4 _aGenome
650 0 4 _aGlucokinase
_xgenetics
650 0 4 _aHumans
650 0 4 _aKruppel-Like Transcription Factors
_xgenetics
650 0 4 _aLimb Deformities, Congenital
_xgenetics
650 0 4 _aMicrosatellite Repeats
650 0 4 _aNerve Tissue Proteins
_xgenetics
650 0 4 _aSyndrome
650 0 4 _aZinc Finger Protein Gli3
700 1 _aWindpassinger, Christian
700 1 _aOfner, Lisa
700 1 _aVincent, John B
700 1 _aCheung, Joseph
700 1 _aScherer, Stephen W
700 1 _aWagner, Klaus
700 1 _aKroisel, Peter M
700 1 _aPetek, Erwin
773 0 _tEuropean journal of medical genetics
_gvol. 49
_gno. 4
_gp. 338-45
856 4 0 _uhttps://doi.org/10.1016/j.ejmg.2005.10.133
_zAvailable from publisher's website
999 _c16420884
_d16420884