Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/7286
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dc.contributor.authorMitchell, C.-
dc.contributor.authorSpeed, C.-
dc.contributor.authorNicholl, J.-
dc.contributor.authorSutherland, G.-
dc.date.issued1996-
dc.identifier.citationGenomics, 1996; 31(1):139-140-
dc.identifier.issn0888-7543-
dc.identifier.issn1089-8646-
dc.identifier.urihttp://hdl.handle.net/2440/7286-
dc.description.statementofresponsibilityMitchell, Christina A. ; Speed, Caroline J. ; Nicholl, Jillian ; Sutherland, Grant R.-
dc.language.isoen-
dc.publisherACADEMIC PRESS INC JNL-COMP SUBSCRIPTIONS-
dc.source.urihttp://dx.doi.org/10.1006/geno.1996.0023-
dc.subjectChromosomes, Human, Pair 10-
dc.subjectX Chromosome-
dc.subjectHumans-
dc.subjectOculocerebrorenal Syndrome-
dc.subjectPhosphoric Monoester Hydrolases-
dc.subjectDNA, Complementary-
dc.subjectIn Situ Hybridization, Fluorescence-
dc.subjectChromosome Mapping-
dc.subjectMale-
dc.subjectGenetic Linkage-
dc.subjectInositol Polyphosphate 5-Phosphatases-
dc.titleChromosomal mapping of the gene (INPP5A) encoding the 43-kDa membrane-associated inositol polyphosphate 5-phosphatase to 10q26.3 by fluorescence in situ hybridization-
dc.typeJournal article-
dc.identifier.doi10.1006/geno.1996.0023-
pubs.publication-statusPublished-
Appears in Collections:Aurora harvest
Paediatrics publications

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