dc.contributor.author | Kaya, Murat | |
dc.contributor.author | Suer, İlknur | |
dc.contributor.author | Karaman, Birsen | |
dc.contributor.author | Palanduz, Şükrü | |
dc.contributor.author | ÇEFLE, Kıvanç | |
dc.contributor.author | Öztürk, Şükrü | |
dc.date.accessioned | 2021-03-06T11:16:43Z | |
dc.date.available | 2021-03-06T11:16:43Z | |
dc.identifier.citation | Kaya 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.", F1000Research, cilt.8, ss.281, 2019 | |
dc.identifier.other | vv_1032021 | |
dc.identifier.other | av_ee3d6359-33e5-449e-aabf-1ade31a1defd | |
dc.identifier.uri | http://hdl.handle.net/20.500.12627/156402 | |
dc.identifier.uri | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85067655751&origin=inward | |
dc.identifier.uri | https://doi.org/10.12688/f1000research.18455.1 | |
dc.language.iso | eng | |
dc.title | 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.type | Makale | |
dc.relation.journal | F1000Research | |
dc.contributor.department | Istanbul Üniversitesi Tıp Fakültesi , , | |
dc.identifier.volume | 8 | |
dc.identifier.startpage | 281 | |
dc.identifier.endpage | 281 | |
dc.contributor.firstauthorID | 335111 | |