000 01880 a2200589 4500
005 20250516022040.0
264 0 _c20110721
008 201107s 0 0 eng d
022 _a1460-2083
024 7 _a10.1093/hmg/ddr031
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aBrouns, Madeleine R
245 0 0 _aOver-expression of Grhl2 causes spina bifida in the Axial defects mutant mouse.
_h[electronic resource]
260 _bHuman molecular genetics
_cApr 2011
300 _a1536-46 p.
_bdigital
500 _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't
650 0 4 _aAnimals
650 0 4 _aCell Proliferation
650 0 4 _aChromosome Mapping
650 0 4 _aChromosomes, Mammalian
_xgenetics
650 0 4 _aFemale
650 0 4 _aGene Silencing
650 0 4 _aGenetic Linkage
650 0 4 _aHumans
650 0 4 _aHybridization, Genetic
650 0 4 _aLower Gastrointestinal Tract
_xabnormalities
650 0 4 _aMale
650 0 4 _aMice
650 0 4 _aMice, Inbred BALB C
650 0 4 _aMice, Inbred C57BL
650 0 4 _aMice, Mutant Strains
650 0 4 _aMutation
650 0 4 _aSpinal Dysraphism
_xembryology
650 0 4 _aTranscription Factors
_xgenetics
650 0 4 _aTranscription, Genetic
650 0 4 _aUp-Regulation
700 1 _aDe Castro, Sandra C P
700 1 _aTerwindt-Rouwenhorst, Els A
700 1 _aMassa, Valentina
700 1 _aHekking, Johan W
700 1 _aHirst, Caroline S
700 1 _aSavery, Dawn
700 1 _aMunts, Chantal
700 1 _aPartridge, Darren
700 1 _aLamers, Wout
700 1 _aKöhler, Eleonore
700 1 _avan Straaten, Henny W
700 1 _aCopp, Andrew J
700 1 _aGreene, Nicholas D E
773 0 _tHuman molecular genetics
_gvol. 20
_gno. 8
_gp. 1536-46
856 4 0 _uhttps://doi.org/10.1093/hmg/ddr031
_zAvailable from publisher's website
999 _c20543659
_d20543659