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Dinucleotide polymorphism at the DXS1178 locus is tightly linked to PGK1 at Xq13

dc.contributor.authorSwaroop, Ananden_US
dc.contributor.authorYang-Feng, Teresa L.en_US
dc.contributor.authorFujita, Ricardoen_US
dc.contributor.authorPakstis, Andrew J.en_US
dc.contributor.authorSkolnick, Craigen_US
dc.date.accessioned2006-09-11T19:13:13Z
dc.date.available2006-09-11T19:13:13Z
dc.date.issued1995-04en_US
dc.identifier.citationFujita, Ricardo; Skolnick, Craig; Pakstis, Andrew J.; Yang-Feng, Teresa L.; Swaroop, Anand; (1995). "Dinucleotide polymorphism at the DXS1178 locus is tightly linked to PGK1 at Xq13." Human Genetics 95(4): 467-468. <http://hdl.handle.net/2027.42/47638>en_US
dc.identifier.issn1432-1203en_US
dc.identifier.issn0340-6717en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/47638
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=7705848&dopt=citationen_US
dc.description.abstractA polymorphic CA repeat (locus name DXS1178 ) was isolated from a 1-megabase YAC (OTCC) containing the OTC gene, located at Xp21.1. However, amplification in human-rodent hybrid cells and segregation analysis in three CEPH families mapped the DXS1178 locus at Xq13. The mapping ambiguity is apparently caused by the chimeric nature of the OTCC YAC clone.en_US
dc.format.extent109243 bytes
dc.format.extent3115 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherSpringer-Verlagen_US
dc.subject.otherHuman Geneticsen_US
dc.subject.otherInternal Medicineen_US
dc.subject.otherMolecular Medicineen_US
dc.subject.otherMetabolic Diseasesen_US
dc.subject.otherBiomedicineen_US
dc.titleDinucleotide polymorphism at the DXS1178 locus is tightly linked to PGK1 at Xq13en_US
dc.typeArticleen_US
dc.subject.hlbsecondlevelMolecular, Cellular and Developmental Biologyen_US
dc.subject.hlbsecondlevelGeneticsen_US
dc.subject.hlbsecondlevelBiological Chemistryen_US
dc.subject.hlbtoplevelScienceen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDepartment of Ophthalmology, Kellogg Eye Center, University of Michigan, 1000 Wall Street, 48 105, Ann Arbor, MI, USA; Department of Human Genetics, Kellogg Eye Center, University of Michigan, 1000 Wall Street, 48 105, Ann Arbor, MI, USAen_US
dc.contributor.affiliationumDepartment of Ophthalmology, Kellogg Eye Center, University of Michigan, 1000 Wall Street, 48 105, Ann Arbor, MI, USAen_US
dc.contributor.affiliationumDepartment of Ophthalmology, Kellogg Eye Center, University of Michigan, 1000 Wall Street, 48 105, Ann Arbor, MI, USAen_US
dc.contributor.affiliationotherDepartment of Genetics, Yale University School of Medicine, 06510, New Haven, CT, USAen_US
dc.contributor.affiliationotherDepartment of Genetics, Yale University School of Medicine, 06510, New Haven, CT, USAen_US
dc.contributor.affiliationumcampusAnn Arboren_US
dc.identifier.pmid7705848en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/47638/1/439_2004_Article_BF00208981.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1007/BF00208981en_US
dc.identifier.sourceHuman Geneticsen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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