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An improved method for detecting Y chromosomal DNA

dc.contributor.authorStalvey, John R. D.en_US
dc.contributor.authorErickson, Robert P.en_US
dc.date.accessioned2006-09-11T19:11:45Z
dc.date.available2006-09-11T19:11:45Z
dc.date.issued1987-07en_US
dc.identifier.citationStalvey, John R. D.; Erickson, Robert P.; (1987). "An improved method for detecting Y chromosomal DNA." Human Genetics 76(3): 240-243. <http://hdl.handle.net/2027.42/47617>en_US
dc.identifier.issn1432-1203en_US
dc.identifier.issn0340-6717en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/47617
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=3036688&dopt=citationen_US
dc.description.abstractThe DNA probe Y97 was derived from a repeat sequence in the human Y centromere, a region which must be present in a mitotically functional Y chromosome. We have demonstrated that Y97, which detects a Y-specific 5.5-kb Eco RI fragment by Southern analysis, is very useful for the molecular detection of small amounts of Y-derived material and represents a significant improvement over previous tests for molecular diagnosis of sex. The male-female difference in hybridization was unequivocal even when only 25 ng of total DNA was used per lane. Furthermore, in mixing experiments the 5.5-kb Eco RI fragment was detectable even when only 5% of the total DNA was male. By increasing hybridization stringency, we have developed a rapid, sensitive, and accurate method to detect Y chromosomal DNA in unrestricted samples.en_US
dc.format.extent655119 bytes
dc.format.extent3115 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherSpringer-Verlagen_US
dc.subject.otherMolecular Medicineen_US
dc.subject.otherBiomedicineen_US
dc.subject.otherHuman Geneticsen_US
dc.subject.otherInternal Medicineen_US
dc.subject.otherMetabolic Diseasesen_US
dc.titleAn improved method for detecting Y chromosomal DNAen_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.affiliationumDivision of Pediatric Genetics, Department of Pediatrics and Communicable Diseases, University of Michigan School of Medicine, 48109-0618, Ann Arbor, MI, USAen_US
dc.contributor.affiliationumDivision of Pediatric Genetics, Department of Pediatrics and Communicable Diseases, University of Michigan School of Medicine, 48109-0618, Ann Arbor, MI, USAen_US
dc.contributor.affiliationumcampusAnn Arboren_US
dc.identifier.pmid3036688en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/47617/1/439_2004_Article_BF00283615.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1007/BF00283615en_US
dc.identifier.sourceHuman Geneticsen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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