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Seven new cases of cayler cardiofacial syndrome with chromosome 22q11.2 deletion, including a familial case Presented in part at The Annual Meeting of the American Society of Human Genetics in 1996.
dc.contributor.authorBawle, Erawati V.en_US
dc.contributor.authorConard, Joan V.en_US
dc.contributor.authorVan Dyke, Daniel L.en_US
dc.contributor.authorCzarnecki, Paulaen_US
dc.contributor.authorDriscoll, Deborah A.en_US
dc.date.accessioned2006-04-19T13:44:07Z
dc.date.available2006-04-19T13:44:07Z
dc.date.issued1998-10-12en_US
dc.identifier.citationBawle, Erawati V.; Conard, Joan; Van Dyke, Daniel L.; Czarnecki, Paula; Driscoll, Deborah A. (1998)."Seven new cases of cayler cardiofacial syndrome with chromosome 22q11.2 deletion, including a familial case Presented in part at The Annual Meeting of the American Society of Human Genetics in 1996. ." American Journal of Medical Genetics 79(5): 406-410. <http://hdl.handle.net/2027.42/34651>en_US
dc.identifier.issn0148-7299en_US
dc.identifier.issn1096-8628en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/34651
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=9779813&dopt=citationen_US
dc.description.abstractNo abstract.en_US
dc.format.extent440741 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.titleSeven new cases of cayler cardiofacial syndrome with chromosome 22q11.2 deletion, including a familial case Presented in part at The Annual Meeting of the American Society of Human Genetics in 1996.en_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.affiliationotherDivision of Genetics, Children's Hospital of Michigan, Wayne State University, Detroit, Michigan ; Department of Medical Genetics, Henry Ford Hospital, Detroit, Michigan ; Division of Genetics, Children's Hospital of Michigan, 3901 Beaubien Boulevard, Detroit, MI 48201en_US
dc.contributor.affiliationotherDivision of Genetics, Children's Hospital of Michigan, Wayne State University, Detroit, Michiganen_US
dc.contributor.affiliationotherDepartment of Medical Genetics, Henry Ford Hospital, Detroit, Michiganen_US
dc.contributor.affiliationotherDepartment of Medical Genetics, Henry Ford Hospital, Detroit, Michiganen_US
dc.contributor.affiliationotherChildren's Hospital of Philadelphia, Philadelphia, Pennsylvaniaen_US
dc.identifier.pmid9779813en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/34651/1/18_ftp.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1002/(SICI)1096-8628(19981012)79:5<406::AID-AJMG18>3.0.CO;2-Ven_US
dc.identifier.sourceAmerican Journal of Medical Geneticsen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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