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Severe anomalies associated with ring chromosome 7
dc.contributor.authorBiesecker, Leslie G.en_US
dc.contributor.authorCox, Beth A.en_US
dc.contributor.authorGlover, Thomas W.en_US
dc.date.accessioned2006-04-28T16:48:32Z
dc.date.available2006-04-28T16:48:32Z
dc.date.issued1991-09-15en_US
dc.identifier.citationBiesecker, Leslie G.; Cox, Beth; Glover, Thomas W. (1991)."Severe anomalies associated with ring chromosome 7." American Journal of Medical Genetics 40(4): 429-431. <http://hdl.handle.net/2027.42/38256>en_US
dc.identifier.issn0148-7299en_US
dc.identifier.issn1096-8628en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/38256
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=1746606&dopt=citationen_US
dc.description.abstractA newborn infant with the polyasplenia sequence, intrauterine growth retardation, cutaneous nevi, and minor anomalies was found to have mosaicism for ring chromosome 7. This patient's anomalies are markedly different from those of previous patients reported with this cytogenetic anomaly.en_US
dc.format.extent362075 bytes
dc.format.extent3118 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherWiley Subscription Services, Inc., A Wiley Companyen_US
dc.subject.otherLife and Medical Sciencesen_US
dc.subject.otherGeneticsen_US
dc.titleSevere anomalies associated with ring chromosome 7en_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelGeneticsen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.subject.hlbtoplevelScienceen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDepartments of Pediatrics and Communicable Diseases, University of Michigan Medical School, Ann Arbor, Michigan ; University of Michigan Department of Pediatrics and Communicable Diseases, D1109 M.P.B. Box 0718, Ann Arbor, MI 48109en_US
dc.contributor.affiliationumDepartment of Pathology, University of Michigan Medical School, Ann Arbor, Michiganen_US
dc.contributor.affiliationumDepartments of Pediatrics and Communicable Diseases, University of Michigan Medical School, Ann Arbor, Michigan ; Department of Human Genetics, University of Michigan Medical School, Ann Arbor, Michiganen_US
dc.identifier.pmid1746606en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/38256/1/1320400410_ftp.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1002/ajmg.1320400410en_US
dc.identifier.sourceAmerican Journal of Medical Geneticsen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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