Please use this identifier to cite or link to this item: https://hdl.handle.net/11499/8798
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dc.contributor.authorBagcı, Gülseren-
dc.contributor.authorÇetin, Gökhan Ozan-
dc.contributor.authorSemerci, Nur-
dc.contributor.authorToruner, G. A.-
dc.contributor.authorCinbiş, Mine-
dc.date.accessioned2019-08-16T12:47:22Z-
dc.date.available2019-08-16T12:47:22Z-
dc.date.issued2012-
dc.identifier.issn0962-8827-
dc.identifier.urihttps://hdl.handle.net/11499/8798-
dc.identifier.urihttps://doi.org/10.1097/MCD.0b013e32834d6ba3-
dc.description.abstractAbstract Not Availableen_US
dc.language.isoenen_US
dc.relation.ispartofClinical Dysmorphologyen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectagenesisen_US
dc.subjectanteverted nostrilen_US
dc.subjectarticleen_US
dc.subjectbirth weighten_US
dc.subjectblepharophimosisen_US
dc.subjectbody heighten_US
dc.subjectbody weighten_US
dc.subjectC bandingen_US
dc.subjectcase reporten_US
dc.subjectchromosome 14qen_US
dc.subjectchromosome breakageen_US
dc.subjectchromosome translocationen_US
dc.subjectchromosome Xpen_US
dc.subjectchromosome Ypen_US
dc.subjectcongenital heart malformationen_US
dc.subjectcorpus callosumen_US
dc.subjectcytogeneticsen_US
dc.subjectDNA microarrayen_US
dc.subjecteye malformationen_US
dc.subjectface dysmorphiaen_US
dc.subjectflatfooten_US
dc.subjectfluorescence in situ hybridizationen_US
dc.subjectgait disorderen_US
dc.subjectgene deletionen_US
dc.subjectgene duplicationen_US
dc.subjectgrowth retardationen_US
dc.subjecthead circumferenceen_US
dc.subjecthearing impairmenten_US
dc.subjectherniaen_US
dc.subjectheterochromatinen_US
dc.subjecthirsutismen_US
dc.subjecthumanen_US
dc.subjecthypertelorismen_US
dc.subjecthypoplasiaen_US
dc.subjectintrauterine growth retardationen_US
dc.subjectkaryotypeen_US
dc.subjectlong philtrumen_US
dc.subjectlow set earen_US
dc.subjectmaleen_US
dc.subjectmental deficiencyen_US
dc.subjectmicrocephalyen_US
dc.subjectmicrognathiaen_US
dc.subjectmuscle hypotoniaen_US
dc.subjectneuroimagingen_US
dc.subjectnose malformationen_US
dc.subjectnuclear magnetic resonance imagingen_US
dc.subjectpalate malformationen_US
dc.subjectpalpebral fissureen_US
dc.subjectpriority journalen_US
dc.subjectptosisen_US
dc.subjectstrabismusen_US
dc.subjectAbnormalities, Multipleen_US
dc.subjectChild, Preschoolen_US
dc.subjectChromosome Aberrationsen_US
dc.subjectChromosome Deletionen_US
dc.subjectChromosomes, Human, Pair 14en_US
dc.subjectCytogenetic Analysisen_US
dc.subjectHumansen_US
dc.subjectIn Situ Hybridization, Fluorescenceen_US
dc.subjectKaryotypingen_US
dc.subjectMaleen_US
dc.subjectSequence Deletionen_US
dc.subjectTranslocation, Geneticen_US
dc.titleTerminal 14q deletion with unbalanced t(Y;14)(q12;q32) translocationen_US
dc.typeArticleen_US
dc.relation.journalClinical Dysmorphologyen_US
dc.identifier.volume21en_US
dc.identifier.issue1en_US
dc.identifier.startpage37en_US
dc.identifier.endpage41en_US
dc.authorid261007973-
dc.identifier.doi10.1097/MCD.0b013e32834d6ba3-
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.identifier.pmid22143350en_US
dc.identifier.scopus2-s2.0-83255181192en_US
dc.identifier.wosWOS:000298148400010en_US
dc.identifier.scopusqualityQ2-
dc.ownerPamukkale University-
item.grantfulltextnone-
item.languageiso639-1en-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.fulltextNo Fulltext-
item.openairetypeArticle-
item.cerifentitytypePublications-
crisitem.author.dept14.02. Internal Medicine-
crisitem.author.dept14.02. Internal Medicine-
crisitem.author.dept14.02. Internal Medicine-
Appears in Collections:PubMed İndeksli Yayınlar Koleksiyonu / PubMed Indexed Publications Collection
Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection
Tıp Fakültesi Koleksiyonu
WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection
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