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dc.contributor.authorBasaran, Seher
dc.contributor.authorToksoy, Guven
dc.contributor.authorKayserili, Hulya
dc.contributor.authorKaraman, Birsen
dc.contributor.authorHas, Recep
dc.contributor.authorUyguner, Zehra Oya
dc.contributor.authorMiny, Peter
dc.contributor.authorYilmaz, Kader
dc.date.accessioned2021-03-04T19:18:56Z
dc.date.available2021-03-04T19:18:56Z
dc.date.issued2019
dc.identifier.citationToksoy G., Karaman B., Uyguner Z. O. , Yilmaz K., Has R., Kayserili H., Miny P., Basaran S., "APPLICATION OF MLPA (MULTIPLEX LIGATION-DEPENDENT PROBE AMPLIFICATION) IN FETUSES WITH AN ABNORMAL SONOGRAM AND NORMAL KARYOTYPE", JOURNAL OF ISTANBUL FACULTY OF MEDICINE-ISTANBUL TIP FAKULTESI DERGISI, cilt.82, ss.5-11, 2019
dc.identifier.othervv_1032021
dc.identifier.otherav_8f218180-2e26-4c94-a9c7-f4b9e3696b67
dc.identifier.urihttp://hdl.handle.net/20.500.12627/96681
dc.identifier.urihttps://doi.org/10.26650/iuitfd.413596
dc.description.abstractObjective/Material and Method: Cryptic chromosomal imbalances contribute significantly to the etiology of multiple congenital anomalies with or without mental retardation (MCA/MR). Current approaches in prenatal diagnosis include targeted high resolution analyses by MLPA and some microarray platforms or a genomewide screening at maximal resolution using oligonucleotide or SNP arrays. The major disadvantages of the latter approach are cost and the inadvertent detection of copy number variation of unknown clinical significance.
dc.language.isoeng
dc.subjectTıp
dc.subjectTemel Tıp Bilimleri
dc.subjectSağlık Bilimleri
dc.subjectKlinik Tıp (MED)
dc.subjectKlinik Tıp
dc.subjectTIP, GENEL & İÇECEK
dc.titleAPPLICATION OF MLPA (MULTIPLEX LIGATION-DEPENDENT PROBE AMPLIFICATION) IN FETUSES WITH AN ABNORMAL SONOGRAM AND NORMAL KARYOTYPE
dc.typeMakale
dc.relation.journalJOURNAL OF ISTANBUL FACULTY OF MEDICINE-ISTANBUL TIP FAKULTESI DERGISI
dc.contributor.departmentİstanbul Üniversitesi , İstanbul Tıp Fakültesi , Dahili Bilimler
dc.identifier.volume82
dc.identifier.issue1
dc.identifier.startpage5
dc.identifier.endpage11
dc.contributor.firstauthorID260708


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