Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/11414
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dc.contributor.authorHollway, G.-
dc.contributor.authorMulley, J.-
dc.date.issued1998-
dc.identifier.citationClinical Genetics: an international journal of genetics and molecular medicine, 1998; 54(2):152-154-
dc.identifier.issn0009-9163-
dc.identifier.issn1399-0004-
dc.identifier.urihttp://hdl.handle.net/2440/11414-
dc.language.isoen-
dc.publisherWiley-
dc.source.urihttp://dx.doi.org/10.1111/j.1399-0004.1998.tb03719.x-
dc.subjectChromosomes, Human, Pair 4-
dc.subjectHumans-
dc.subjectGrowth Disorders-
dc.subjectHomeodomain Proteins-
dc.subjectTranscription Factors-
dc.subjectAmino Acid Substitution-
dc.subjectHeteroduplex Analysis-
dc.subjectSequence Deletion-
dc.subjectPolymorphism, Genetic-
dc.subjectPolymorphism, Single-Stranded Conformational-
dc.subjectGenes, Homeobox-
dc.subjectIntrons-
dc.subjectExons-
dc.subjectMSX1 Transcription Factor-
dc.subjectGenetic Variation-
dc.titlePolymorphic variants within the homeobox gene MSX1: a candidate gene for developmental disorders.-
dc.typeJournal article-
dc.identifier.doi10.1111/j.1399-0004.1998.tb03719.x-
pubs.publication-statusPublished-
Appears in Collections:Aurora harvest 2
Genetics publications

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