dc.contributor.author | Yakut Uzuner, Sezin | |
dc.contributor.author | Şimşek, M | |
dc.contributor.author | Karaman, Birsen | |
dc.contributor.author | Karaüzüm, Sibel | |
dc.contributor.author | Sanhal, Cem Yaşar | |
dc.contributor.author | Çetin, Zafer | |
dc.date.accessioned | 2021-12-10T11:31:33Z | |
dc.date.available | 2021-12-10T11:31:33Z | |
dc.date.issued | 2015 | |
dc.identifier.citation | Yakut Uzuner S., Çetin Z., Sanhal C. Y. , Karaüzüm S., Karaman B., Şimşek M., "PRENATAL DIAGNOSIS OF DE NOVO SUPERNUMERARY MARKER CHROMOSOME ORIGINATED FROM CHROMOSOME 16 BY ARRAY-CGH", Genetic Counseling, cilt.26, sa.3, ss.299-305, 2015 | |
dc.identifier.issn | 1015-8146 | |
dc.identifier.other | vv_1032021 | |
dc.identifier.other | av_83621798-1e79-46c8-946a-a22bfc1019c3 | |
dc.identifier.uri | http://hdl.handle.net/20.500.12627/172059 | |
dc.description.abstract | A 33 years-old pregnant woman was referred for amniocentesis at 19 weeks of gestation due to abnormal serum biochemistry. A non-satellited, monocentric marker chromosome was observed with a frequency of 50% in cultured amniocytes. Parental karyotypes were normal. The marker chromosome was found to be derived from chromosome 16 by FISH and array-CGH analysis. Genetic counseling was given to parents and the family decided to terminate the pregnancy. Dysmorphic findings including; low set ears, exophtalmos depressed nasal bridge, large mouth and lips, posture anomalies at the extremities were detected at autopsy. | |
dc.language.iso | eng | |
dc.subject | Pathophysiology | |
dc.subject | Tıp | |
dc.subject | Sağlık Bilimleri | |
dc.subject | Dahili Tıp Bilimleri | |
dc.subject | Tıbbi Genetik | |
dc.subject | Genetics | |
dc.subject | Family Practice | |
dc.subject | Genetics (clinical) | |
dc.subject | Fundamentals and Skills | |
dc.subject | General Health Professions | |
dc.subject | Internal Medicine | |
dc.subject | Health Sciences | |
dc.subject | Life Sciences | |
dc.subject | General Medicine | |
dc.subject | Medicine (miscellaneous) | |
dc.subject | Assessment and Diagnosis | |
dc.subject | Klinik Tıp (MED) | |
dc.subject | Yaşam Bilimleri (LIFE) | |
dc.subject | Klinik Tıp | |
dc.subject | Moleküler Biyoloji ve Genetik | |
dc.subject | TIP, GENEL & İÇECEK | |
dc.subject | GENETİK VE HAYAT | |
dc.title | PRENATAL DIAGNOSIS OF DE NOVO SUPERNUMERARY MARKER CHROMOSOME ORIGINATED FROM CHROMOSOME 16 BY ARRAY-CGH | |
dc.type | Makale | |
dc.relation.journal | Genetic Counseling | |
dc.contributor.department | Akdeniz Üniversitesi , Tıp Fakültesi , Temel Tıp Bilimleri Bölümü | |
dc.identifier.volume | 26 | |
dc.identifier.issue | 3 | |
dc.identifier.startpage | 299 | |
dc.identifier.endpage | 305 | |
dc.contributor.firstauthorID | 2706384 | |