Please use this identifier to cite or link to this item:
https://hdl.handle.net/11499/8798
Full metadata record
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Bagcı, Gülseren | - |
dc.contributor.author | Çetin, Gökhan Ozan | - |
dc.contributor.author | Semerci, Nur | - |
dc.contributor.author | Toruner, G. A. | - |
dc.contributor.author | Cinbiş, Mine | - |
dc.date.accessioned | 2019-08-16T12:47:22Z | - |
dc.date.available | 2019-08-16T12:47:22Z | - |
dc.date.issued | 2012 | - |
dc.identifier.issn | 0962-8827 | - |
dc.identifier.uri | https://hdl.handle.net/11499/8798 | - |
dc.identifier.uri | https://doi.org/10.1097/MCD.0b013e32834d6ba3 | - |
dc.description.abstract | Abstract Not Available | en_US |
dc.language.iso | en | en_US |
dc.relation.ispartof | Clinical Dysmorphology | en_US |
dc.rights | info:eu-repo/semantics/closedAccess | en_US |
dc.subject | agenesis | en_US |
dc.subject | anteverted nostril | en_US |
dc.subject | article | en_US |
dc.subject | birth weight | en_US |
dc.subject | blepharophimosis | en_US |
dc.subject | body height | en_US |
dc.subject | body weight | en_US |
dc.subject | C banding | en_US |
dc.subject | case report | en_US |
dc.subject | chromosome 14q | en_US |
dc.subject | chromosome breakage | en_US |
dc.subject | chromosome translocation | en_US |
dc.subject | chromosome Xp | en_US |
dc.subject | chromosome Yp | en_US |
dc.subject | congenital heart malformation | en_US |
dc.subject | corpus callosum | en_US |
dc.subject | cytogenetics | en_US |
dc.subject | DNA microarray | en_US |
dc.subject | eye malformation | en_US |
dc.subject | face dysmorphia | en_US |
dc.subject | flatfoot | en_US |
dc.subject | fluorescence in situ hybridization | en_US |
dc.subject | gait disorder | en_US |
dc.subject | gene deletion | en_US |
dc.subject | gene duplication | en_US |
dc.subject | growth retardation | en_US |
dc.subject | head circumference | en_US |
dc.subject | hearing impairment | en_US |
dc.subject | hernia | en_US |
dc.subject | heterochromatin | en_US |
dc.subject | hirsutism | en_US |
dc.subject | human | en_US |
dc.subject | hypertelorism | en_US |
dc.subject | hypoplasia | en_US |
dc.subject | intrauterine growth retardation | en_US |
dc.subject | karyotype | en_US |
dc.subject | long philtrum | en_US |
dc.subject | low set ear | en_US |
dc.subject | male | en_US |
dc.subject | mental deficiency | en_US |
dc.subject | microcephaly | en_US |
dc.subject | micrognathia | en_US |
dc.subject | muscle hypotonia | en_US |
dc.subject | neuroimaging | en_US |
dc.subject | nose malformation | en_US |
dc.subject | nuclear magnetic resonance imaging | en_US |
dc.subject | palate malformation | en_US |
dc.subject | palpebral fissure | en_US |
dc.subject | priority journal | en_US |
dc.subject | ptosis | en_US |
dc.subject | strabismus | en_US |
dc.subject | Abnormalities, Multiple | en_US |
dc.subject | Child, Preschool | en_US |
dc.subject | Chromosome Aberrations | en_US |
dc.subject | Chromosome Deletion | en_US |
dc.subject | Chromosomes, Human, Pair 14 | en_US |
dc.subject | Cytogenetic Analysis | en_US |
dc.subject | Humans | en_US |
dc.subject | In Situ Hybridization, Fluorescence | en_US |
dc.subject | Karyotyping | en_US |
dc.subject | Male | en_US |
dc.subject | Sequence Deletion | en_US |
dc.subject | Translocation, Genetic | en_US |
dc.title | Terminal 14q deletion with unbalanced t(Y;14)(q12;q32) translocation | en_US |
dc.type | Article | en_US |
dc.relation.journal | Clinical Dysmorphology | en_US |
dc.identifier.volume | 21 | en_US |
dc.identifier.issue | 1 | en_US |
dc.identifier.startpage | 37 | en_US |
dc.identifier.endpage | 41 | en_US |
dc.authorid | 261007973 | - |
dc.identifier.doi | 10.1097/MCD.0b013e32834d6ba3 | - |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
dc.identifier.pmid | 22143350 | en_US |
dc.identifier.scopus | 2-s2.0-83255181192 | en_US |
dc.identifier.wos | WOS:000298148400010 | en_US |
dc.identifier.scopusquality | Q2 | - |
dc.owner | Pamukkale University | - |
item.grantfulltext | none | - |
item.languageiso639-1 | en | - |
item.openairecristype | http://purl.org/coar/resource_type/c_18cf | - |
item.fulltext | No Fulltext | - |
item.openairetype | Article | - |
item.cerifentitytype | Publications | - |
crisitem.author.dept | 14.02. Internal Medicine | - |
crisitem.author.dept | 14.02. Internal Medicine | - |
crisitem.author.dept | 14.02. 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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