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Identification of critical regions for clinical features of distal 10q deletion syndrome
dc.contributor.authorYatsenko,en_US
dc.contributor.authorKruer,en_US
dc.contributor.authorBader,en_US
dc.contributor.authorCorzo,en_US
dc.contributor.authorSchuette,en_US
dc.contributor.authorKeegan,en_US
dc.contributor.authorNowakowska,en_US
dc.contributor.authorPeacock,en_US
dc.contributor.authorCai,en_US
dc.contributor.authorPeiffer,en_US
dc.contributor.authorGunderson,en_US
dc.contributor.authorOu,en_US
dc.contributor.authorChinault,en_US
dc.contributor.authorCheung,en_US
dc.date.accessioned2010-04-01T14:54:18Z
dc.date.available2010-04-01T14:54:18Z
dc.date.issued2009-07en_US
dc.identifier.citationYatsenko, ; Kruer, ; Bader, ; Corzo, ; Schuette, ; Keegan, ; Nowakowska, ; Peacock, ; Cai, ; Peiffer, ; Gunderson, ; Ou, ; Chinault, ; Cheung, (2009). "Identification of critical regions for clinical features of distal 10q deletion syndrome." Clinical Genetics 76(1): 54-62. <http://hdl.handle.net/2027.42/65360>en_US
dc.identifier.issn0009-9163en_US
dc.identifier.issn1399-0004en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/65360
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=19558528&dopt=citationen_US
dc.format.extent644706 bytes
dc.format.extent3110 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.publisherBlackwell Publishing Ltden_US
dc.rights© 2009 John Wiley & Sons A/Sen_US
dc.subject.otherArray Comparative Genomic Hybridizationen_US
dc.subject.otherChromosome Rearrangementen_US
dc.subject.otherCritical Regionen_US
dc.subject.otherDeletion 10qen_US
dc.subject.otherDOCK1 Geneen_US
dc.subject.otherGenotype-phenotype Correlationen_US
dc.titleIdentification of critical regions for clinical features of distal 10q deletion syndromeen_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelGeneticsen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDepartment of Pediatrics, Division of Genetics, University of Michigan, Ann Arbor, MI, USAen_US
dc.contributor.affiliationotherDepartment of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USAen_US
dc.contributor.affiliationotherDepartment of Pediatrics, Phoenix Children’s Hospital, Phoenix, AZ, USAen_US
dc.contributor.affiliationotherDepartment of Pediatrics, Maricopa Medical Center, Phoenix, AZ, USAen_US
dc.contributor.affiliationotherNortheast Indiana Genetic Counseling Center, Parkview Hospital, Fort Wayne, IN, USAen_US
dc.contributor.affiliationotherDivision of Clinical Genetics, Boston Children’s Hospital, Boston, MA, USAen_US
dc.contributor.affiliationotherDepartment of Medical Genetics, Institute of Mother and Child, Warsaw, Polanden_US
dc.contributor.affiliationotherIllumina, Inc, San Diego, CA, USAen_US
dc.identifier.pmid19558528en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/65360/1/j.1399-0004.2008.01115.x.pdf
dc.identifier.doi10.1111/j.1399-0004.2008.01115.xen_US
dc.identifier.sourceClinical Geneticsen_US
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dc.owningcollnameInterdisciplinary and Peer-Reviewed


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