Hollway, G.Mulley, J.2006-07-052006-07-051998Clinical Genetics, 1998; 54(2):152-1540009-91631399-0004http://hdl.handle.net/2440/11414enChromosomes, Human, Pair 4HumansGrowth DisordersHomeodomain ProteinsTranscription FactorsAmino Acid SubstitutionHeteroduplex AnalysisSequence DeletionPolymorphism, GeneticPolymorphism, Single-Stranded ConformationalGenes, HomeoboxIntronsExonsMSX1 Transcription FactorGenetic VariationPolymorphic variants within the homeobox gene MSX1: a candidate gene for developmental disorders.Journal article0030004330001998211510.1111/j.1399-0004.1998.tb03719.x2-s2.0-003171599668336