Publication:
Heterozygous 5p13.3-13.2 deletion in a patient with type I Chiari malformation and bilateral Duane retraction syndrome

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dc.contributor.authorBAYRAKLI, FATİH
dc.contributor.authorsBayrakli, F.; Bilguvar, K.; Ceyhan, D.; Ercan-Sencicek, A. G.; Cankaya, T.; Bayrakli, S.; Guney, I.; Mane, S. M.; State, M. W.; Gunel, M.
dc.date.accessioned2022-04-25T00:10:34Z
dc.date.accessioned2026-01-11T15:11:39Z
dc.date.available2022-04-25T00:10:34Z
dc.date.issued2010
dc.identifier.doi10.1111/j.1399-0004.2010.01411.x
dc.identifier.issn0009-9163
dc.identifier.pubmed20447154
dc.identifier.urihttps://hdl.handle.net/11424/263713
dc.identifier.wosWOS:000276489700013
dc.languageeng
dc.publisherWILEY-BLACKWELL
dc.relation.ispartofCLINICAL GENETICS
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectNATRIURETIC-PEPTIDE
dc.subjectBLOOD-PRESSURE
dc.subjectRECEPTOR GENE
dc.subjectHYPERTENSION
dc.subjectHISTORY
dc.subjectNUMBER
dc.titleHeterozygous 5p13.3-13.2 deletion in a patient with type I Chiari malformation and bilateral Duane retraction syndrome
dc.typeother
dc.type.subletter
dspace.entity.typePublication
oaire.citation.endPage502
oaire.citation.issue5
oaire.citation.startPage499
oaire.citation.titleCLINICAL GENETICS
oaire.citation.volume77

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