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Case Report: a novel chromosomal insertion, 46, XY, inv ins(18;2)(q11.2;q13q22), in a patient with infertility and mild intellectual disability

dc.contributor.authorÖztürk, Şükrü
dc.contributor.authorSuer, İlknur
dc.contributor.authorKaraman, Birsen
dc.contributor.authorÇefle, Kıvanç
dc.contributor.authorKaya, Murat
dc.contributor.authorPalanduz, Şükrü
dc.date.accessioned2021-03-05T09:00:57Z
dc.date.available2021-03-05T09:00:57Z
dc.identifier.citationKaya M., Suer İ., Öztürk Ş., Çefle K., Karaman B., Palanduz Ş., "Case Report: a novel chromosomal insertion, 46, XY, inv ins(18;2)(q11.2;q13q22), in a patient with infertility and mild intellectual disability", Diğer, ss.1-12, 2019
dc.identifier.othervv_1032021
dc.identifier.otherav_9bd4c724-3785-4485-a392-55580b180e20
dc.identifier.urihttp://hdl.handle.net/20.500.12627/104759
dc.identifier.urihttps://www.researchgate.net/publication/331690067_Case_Report_a_novel_chromosomal_insertion_46_XY_inv_ins182q112q13q22_in_a_patient_with_infertility_and_mild_intellectual_disability
dc.language.isoeng
dc.subjectGENETİK VE HAYAT
dc.subjectTıp
dc.subjectSağlık Bilimleri
dc.subjectDahili Tıp Bilimleri
dc.subjectTıbbi Genetik
dc.subjectMoleküler Biyoloji ve Genetik
dc.subjectTIP, GENEL & İÇECEK
dc.subjectKlinik Tıp
dc.subjectYaşam Bilimleri (LIFE)
dc.subjectKlinik Tıp (MED)
dc.titleCase Report: a novel chromosomal insertion, 46, XY, inv ins(18;2)(q11.2;q13q22), in a patient with infertility and mild intellectual disability
dc.typeDiğer Yayınlar
dc.contributor.departmentİstanbul Üniversitesi , İstanbul Tıp Fakültesi , Dahili Tıp Bilimleri
dc.contributor.firstauthorID729312


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