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Two highly polymorphic CA repeats in the Menkes gene (ATP7A)
dc.contributor.authorGlover, Thomas W.en_US
dc.contributor.authorInnis, Jeffrey W.en_US
dc.contributor.authorDierick, Herman A.en_US
dc.contributor.authorBegy, Catherine R.en_US
dc.date.accessioned2006-09-11T19:13:25Z
dc.date.available2006-09-11T19:13:25Z
dc.date.issued1995-09en_US
dc.identifier.citationBegy, Catherine R.; Dierick, Herman A.; Innis, Jeffrey W.; Glover, Thomas W.; (1995). "Two highly polymorphic CA repeats in the Menkes gene (ATP7A)." Human Genetics 96(3): 355-356. <http://hdl.handle.net/2027.42/47641>en_US
dc.identifier.issn0340-6717en_US
dc.identifier.issn1432-1203en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/47641
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=7649557&dopt=citationen_US
dc.description.abstractTwo highly polymorphic CA repeats have been identified in the Menkes gene ( ATP7A ). These repeats should be useful for prenatal diagnosis and carrier detection in families with Menkes disease and X-linked cutis laxa. The observed heterozygosity for these two repeats was 0.778 and 0.60 in Centre d'Etude du Polymorphisme Humaine (CEPH) families.en_US
dc.format.extent147024 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.otherMetabolic Diseasesen_US
dc.subject.otherInternal Medicineen_US
dc.subject.otherMolecular Medicineen_US
dc.subject.otherBiomedicineen_US
dc.titleTwo highly polymorphic CA repeats in the Menkes gene (ATP7A)en_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 Pediatrics and Department of Human Genetics, University of Michigan, 4708 Medical Sciences II, Box 0618, 48109, Ann Arbor, MI, USAen_US
dc.contributor.affiliationumDepartment of Pediatrics and Department of Human Genetics, University of Michigan, 4708 Medical Sciences II, Box 0618, 48109, Ann Arbor, MI, USAen_US
dc.contributor.affiliationumDepartment of Pediatrics and Department of Human Genetics, University of Michigan, 4708 Medical Sciences II, Box 0618, 48109, Ann Arbor, MI, USAen_US
dc.contributor.affiliationumDepartment of Pediatrics and Department of Human Genetics, University of Michigan, 4708 Medical Sciences II, Box 0618, 48109, Ann Arbor, MI, USAen_US
dc.contributor.affiliationumcampusAnn Arboren_US
dc.identifier.pmid7649557en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/47641/1/439_2004_Article_BF00210423.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1007/BF00210423en_US
dc.identifier.sourceHuman Geneticsen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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