Polymorphic variants within the homeobox gene MSX1: a candidate gene for developmental disorders.

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dc.contributor.authorHollway, G.
dc.contributor.authorMulley, J.
dc.date.issued1998
dc.identifier.citationClinical Genetics, 1998; 54(2):152-154
dc.identifier.doi10.1111/j.1399-0004.1998.tb03719.x
dc.identifier.issn0009-9163
dc.identifier.issn1399-0004
dc.identifier.urihttp://hdl.handle.net/2440/11414
dc.language.isoen
dc.publisherWiley
dc.source.urihttps://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
pubs.publication-statusPublished

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