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Organ asymmetries as correlates of other anomalies

dc.contributor.authorBarr, Masonen_US
dc.date.accessioned2006-04-19T13:44:23Z
dc.date.available2006-04-19T13:44:23Z
dc.date.issued2001-07-15en_US
dc.identifier.citationBarr, Mason (2001)."Organ asymmetries as correlates of other anomalies." American Journal of Medical Genetics 101(4): 328-333. <http://hdl.handle.net/2027.42/34657>en_US
dc.identifier.issn0148-7299en_US
dc.identifier.issn1096-8628en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/34657
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=11471155&dopt=citationen_US
dc.description.abstractFetuses with deviations in the normal left versus right weight relationships of the paired viscera were examined for correlation with particular malformations, syndromes, or other common factors. Alterations of the normal pattern were observed among cases with cytogenetic anomalies, diaphragmatic hernia, renal duplication, dyshydramnios, and single umbilical artery. A reversal of the left versus right weight pattern was found in the adrenals of cases with hepatic situs inversus but not in those with heterotaxic cardiac lesions. Recipient twins in the twin–twin transfusion syndrome had reduced left lung weights, presumably because of inhibition of lung growth by the enlarged heart. The side of umbilical artery absence did not predict either the nature or complexity of associated malformations. However, it is suggestive that there is discordance between the side of the missing artery and unilateral renal abnormality and that there is preferential absence of the right or left artery, depending on the karyotype. © 2001 Wiley-Liss, Inc.en_US
dc.format.extent191956 bytes
dc.format.extent3118 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherJohn Wiley & Sons, Inc.en_US
dc.subject.otherLife and Medical Sciencesen_US
dc.subject.otherGeneticsen_US
dc.titleOrgan asymmetries as correlates of other anomaliesen_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, Pathology, and Obstetrics, University of Michigan, Ann Arbor, Michigan ; Pediatric Genetics-Teratology, 1924 Taubman Center, Box 0318, University of Michigan Hospitals, Ann Arbor, MI 48109.en_US
dc.identifier.pmid11471155en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/34657/1/1218_ftp.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1002/1096-8628(20010715)101:4<328::AID-AJMG1218>3.0.CO;2-Ken_US
dc.identifier.sourceAmerican Journal of Medical Geneticsen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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