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A CASE REPORT OF A RARE NONSENSE ZP1 VARIANT IN A PATIENT WITH OOCYTE MATURATION DEFECT

dc.contributor.authorBaşaran, Seher
dc.contributor.authorUyguner, Zehra Oya
dc.contributor.authorKaraman, Birsen
dc.contributor.authorBerkay, Ezgi Gizem
dc.date.accessioned2023-10-10T12:17:21Z
dc.date.available2023-10-10T12:17:21Z
dc.date.issued2023
dc.identifier.citationBerkay E. G., Karaman B., Uyguner Z. O., Başaran S., "A CASE REPORT OF A RARE NONSENSE ZP1 VARIANT IN A PATIENT WITH OOCYTE MATURATION DEFECT", JOURNAL OF ISTANBUL FACULTY OF MEDICINE-ISTANBUL TIP FAKULTESI DERGISI, cilt.86, sa.3, ss.264-268, 2023
dc.identifier.issn1305-6433
dc.identifier.othervv_1032021
dc.identifier.otherav_1dec163e-1744-45b4-8873-292b850d9e84
dc.identifier.urihttp://hdl.handle.net/20.500.12627/190023
dc.identifier.urihttps://doi.org/10.26650/iuitfd.1303555
dc.language.isoeng
dc.subjectGenetik (klinik)
dc.subjectAile Sağlığı
dc.subjectTıp (çeşitli)
dc.subjectGenel Tıp
dc.subjectYaşam Bilimleri
dc.subjectGenetik
dc.subjectKlinik Tıp (MED)
dc.subjectYaşam Bilimleri (LIFE)
dc.subjectKlinik Tıp
dc.subjectMoleküler Biyoloji ve Genetik
dc.subjectTIP, GENEL & DAHİLİ
dc.subjectGENETİK VE KALITIM
dc.subjectTıp
dc.subjectDahili Tıp Bilimleri
dc.subjectTıbbi Genetik
dc.subjectSağlık Bilimleri
dc.subjectGenel Sağlık Meslekleri
dc.subjectPatofizyoloji
dc.subjectTemel Bilgi ve Beceriler
dc.subjectDeğerlendirme ve Teşhis
dc.subjectDahiliye
dc.titleA CASE REPORT OF A RARE NONSENSE ZP1 VARIANT IN A PATIENT WITH OOCYTE MATURATION DEFECT
dc.typeMakale
dc.relation.journalJOURNAL OF ISTANBUL FACULTY OF MEDICINE-ISTANBUL TIP FAKULTESI DERGISI
dc.contributor.department, ,
dc.identifier.volume86
dc.identifier.issue3
dc.identifier.startpage264
dc.identifier.endpage268
dc.contributor.firstauthorID4403441


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