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dc.contributor.authorBozatli, Leyla
dc.contributor.authorAkkopru, Hilal
dc.contributor.authorAykutlu, Hasan Cem
dc.contributor.authorCelik, Zeki
dc.contributor.authorBerberoglu, Kivanc Kudret
dc.contributor.authorGÖRKER, IŞIK
dc.contributor.authorGÜRKAN, HAKAN
dc.contributor.authorUlusal, Selma
dc.contributor.authorATLI, ENGİN
dc.contributor.authorAyaz, Guclu
dc.contributor.authorCeylan, Cansin
dc.contributor.authorTOZKIR, HİLMİ
dc.contributor.authorAraz Altay, Menguhan
dc.contributor.authorErol, Ali
dc.contributor.authorYildiz, Nazike
dc.contributor.authorDirek, Ceren
dc.contributor.authorKilit, Neriman
dc.date.accessioned2021-03-03T09:49:55Z
dc.date.available2021-03-03T09:49:55Z
dc.date.issued2018
dc.identifier.citationGÖRKER I., GÜRKAN H., Ulusal S., ATLI E., Ayaz G., Ceylan C., TOZKIR H., Araz Altay M., Erol A., Yildiz N., et al., "Investigation of Copy Number Variation by arrayCGH in Turkish Children and Adolescents Diagnosed with Autism Spectrum Disorders", NOROPSIKIYATRI ARSIVI-ARCHIVES OF NEUROPSYCHIATRY, cilt.55, sa.3, ss.215-219, 2018
dc.identifier.issn1300-0667
dc.identifier.othervv_1032021
dc.identifier.otherav_1f1efbdf-daa3-4190-8b08-91ea6cc8bc44
dc.identifier.urihttp://hdl.handle.net/20.500.12627/26057
dc.identifier.urihttps://doi.org/10.5152/npa.2017.21611
dc.description.abstractAim: The development of whole-genome screening methodologies for the detection of copy number variations (CNVs), such as array-based comparative genomic hybridization (aCHG), provides a much higher resolution than karyotyping leading to the identification of novel microdeletion and microduptication syndromes often associated with an autism spectrum disease (ASD) phenotype. The aim of the study was to determine CNVs of patients with ASD by using array-based comparative genomic hybridization.
dc.language.isoeng
dc.subjectSağlık Bilimleri
dc.subjectDahili Tıp Bilimleri
dc.subjectNöroloji
dc.subjectTıp
dc.subjectKlinik Tıp (MED)
dc.subjectKlinik Tıp
dc.subjectKLİNİK NEUROLOJİ
dc.titleInvestigation of Copy Number Variation by arrayCGH in Turkish Children and Adolescents Diagnosed with Autism Spectrum Disorders
dc.typeMakale
dc.relation.journalNOROPSIKIYATRI ARSIVI-ARCHIVES OF NEUROPSYCHIATRY
dc.contributor.departmentTrakya Üniversitesi , Tıp Fakültesi , Çocuk Ve Ergen Ruh Sağlığı Ve Hastalıkları Anabilim Dalı
dc.identifier.volume55
dc.identifier.issue3
dc.identifier.startpage215
dc.identifier.endpage219
dc.contributor.firstauthorID256351


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