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A familial form of convulsive disorder with or without mental retardation limited to females: extension of a pedigree limits possible genetic mechanisms
dc.contributor.authorFabisiak, Keithen_US
dc.contributor.authorErickson, Robert P.en_US
dc.date.accessioned2010-04-01T15:39:36Z
dc.date.available2010-04-01T15:39:36Z
dc.date.issued1990-11en_US
dc.identifier.citationFabisiak, Keith; Erickson, Robert P. (1990). "A familial form of convulsive disorder with or without mental retardation limited to females: extension of a pedigree limits possible genetic mechanisms." Clinical Genetics 38(5): 353-358. <http://hdl.handle.net/2027.42/66148>en_US
dc.identifier.issn0009-9163en_US
dc.identifier.issn1399-0004en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/66148
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=2126489&dopt=citationen_US
dc.format.extent430315 bytes
dc.format.extent3110 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.publisherBlackwell Publishing Ltden_US
dc.rights1990 Blackwell Munksgaarden_US
dc.subject.otherEpilepsyen_US
dc.subject.otherFemale-limited Mental Retardationen_US
dc.subject.otherSeizuresen_US
dc.subject.otherSex-limited Gene Expressionen_US
dc.subject.otherSexual Differentiation of Brainen_US
dc.titleA familial form of convulsive disorder with or without mental retardation limited to females: extension of a pedigree limits possible genetic mechanismsen_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelGeneticsen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDepartments of Pediatrics and Communicable Diseases, Ann Arbor, Michigan, USAen_US
dc.contributor.affiliationumHuman Genetics, University of Michigan School of Medicine, Ann Arbor, Michigan, USAen_US
dc.identifier.pmid2126489en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/66148/1/j.1399-0004.1990.tb03594.x.pdf
dc.identifier.doi10.1111/j.1399-0004.1990.tb03594.xen_US
dc.identifier.sourceClinical Geneticsen_US
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dc.owningcollnameInterdisciplinary and Peer-Reviewed


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