Yayın:
A case of de novo mosaic 18q21.3 deletion with a mild phenotype

Basit Görünüm
dc.contributor.authorAlp, Muhammed Yunus
dc.contributor.authorÇebi, Alper Han
dc.contributor.authorSeyhan, S.
dc.contributor.authorCansu, Ali
dc.contributor.authorİkbal, Mevlit
dc.contributor.buuauthoryok
dc.date.accessioned2024-01-15T06:45:33Z
dc.date.available2024-01-15T06:45:33Z
dc.date.issued2014
dc.identifier.citationAlp, M. Y. vd. (2014). "A case of de novo mosaic 18q21.3 deletion with a mild phenotype". Genetic Counseling, 25(1), 71-73.
dc.identifier.endpage73
dc.identifier.issn1015-8146
dc.identifier.issue1
dc.identifier.pubmed24783659
dc.identifier.scopus2-s2.0-84899083814
dc.identifier.startpage71
dc.identifier.urihttps://hdl.handle.net/11452/39014
dc.identifier.volume25
dc.identifier.wos000337197500012
dc.indexed.wosSCIE
dc.language.isoen
dc.publisherMedecine Et Hygiene
dc.relation.journalGenetic Counseling
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectChromosome 18q
dc.subjectBiotechnology & applied microbiology
dc.subjectGenetics & heredity
dc.subjectResearch & experimental medicine
dc.subjectMedical ethics
dc.subject.emtree18q deletion syndrome
dc.subject.emtreeBody height
dc.subject.emtreeBody weight
dc.subject.emtreeCase report
dc.subject.emtreeChild
dc.subject.emtreeChromosome 18q
dc.subject.emtreeChromosome aberration
dc.subject.emtreeChromosome analysis
dc.subject.emtreeDenver developmental screening test
dc.subject.emtreeDevelopmental disorder
dc.subject.emtreeEchocardiography
dc.subject.emtreeEchography
dc.subject.emtreeEczema
dc.subject.emtreeFace dysmorphia
dc.subject.emtreeFoot malformation
dc.subject.emtreeGestational age
dc.subject.emtreeHead circumference
dc.subject.emtreeHuman
dc.subject.emtreeHypospadias
dc.subject.emtreeLetter
dc.subject.emtreeMale
dc.subject.emtreeMedical genetics
dc.subject.emtreeMental deficiency
dc.subject.emtreeMosaicism
dc.subject.emtreeMotor retardation
dc.subject.emtreeNuclear magnetic resonance imaging
dc.subject.emtreeNystagmus
dc.subject.emtreePatient referral
dc.subject.emtreePes equinovarus
dc.subject.emtreePhenotype
dc.subject.emtreePregnancy
dc.subject.emtreePreschool child
dc.subject.emtreeVaginal delivery
dc.subject.meshChild, preschool
dc.subject.meshChromosome deletion
dc.subject.meshChromosome disorders
dc.subject.meshChromosomes, human, pair 18
dc.subject.meshDevelopmental disabilities
dc.subject.meshHumans
dc.subject.meshMale
dc.subject.meshMosaicism
dc.subject.meshPhenotype
dc.subject.wosBiotechnology & applied microbiology
dc.subject.wosMedicine, research & experimental
dc.subject.wosGenetics & heredity
dc.subject.wosMedical ethics
dc.titleA case of de novo mosaic 18q21.3 deletion with a mild phenotype
dc.typeArticle
dc.wos.quartileQ4
dspace.entity.typePublication
local.indexed.atWOS
local.indexed.atScopus

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