Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Tülay Tos"'
Autor:
Tülay Tos, Enis Özkaya, Vakkas Korkmaz, Yeşim Özkaya, Ajlan Tukun, Oya Gökmen, Tuncay Küçüközkan
Publikováno v:
Gynecology Obstetrics & Reproductive Medicine, Vol 18, Iss 3 (2012)
OBJECTIVE: We sought to determine the value of well defined screening method in predicting trisomy cases in our institution. STUDY DESIGN: Totally 300 amniocentesis cases were screened from prospectively collected database. Subjects were referred to
Externí odkaz:
https://doaj.org/article/1773e192dced4127864ec9284e140278
Publikováno v:
Haseki Tıp Bülteni, Vol 49, Iss 1, Pp 37-38 (2011)
Externí odkaz:
https://doaj.org/article/fe813abb36ce4a0c83580528afc1ef33
Publikováno v:
The Tohoku Journal of Experimental Medicine. 206:299-304
Thallium-201 (201Tl) has been widely used as a nuclear reagent for myocardial blood flow imaging. The purpose of this study was to investigate genotoxic effects of 201Tl in patients with angina pectoris (n = 21), who had undergone myocardial perfusio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::62bd97291290292503f5d7063a1d04c5
https://doi.org/10.1620/tjem.206.299
https://doi.org/10.1620/tjem.206.299
Publikováno v:
Turkiye Klinikleri Journal of Medical Sciences. 33:588-590
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::61a9be63344ab74e1b0a2d1fc4601182
https://doi.org/10.5336/medsci.2011-26702
https://doi.org/10.5336/medsci.2011-26702
Publikováno v:
Olgu Ek Sayısı-2014; Volume:, Issue: 3-5
Ankara Medical Journal
Ankara Medical Journal
ÖzetCornelia de Lange sendromu (CDL) karekteristik atipik yüz bulguları, prenatal ve postnatal gelişme geriliği ve zeka geriliği ile karakterizedir. Diğer bir adı Brachman de Lange sendromu diye geçmektedir. 1/10000-1/60000 sıklığında g
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::46f58e252cadfd8ad12f6032e250d838
https://dergipark.org.tr/tr/pub/amj/issue/1748/21551
https://dergipark.org.tr/tr/pub/amj/issue/1748/21551
Publikováno v:
Annals of the Rheumatic Diseases. 62:775-777
The analysis of sister chromatid exchange (SCE) is a cytogenetic technique used to show DNA damage due to an exchange of DNA fragments between sister chromatids.To determine whether HLA-B27 positive patients with ankylosing spondylitis (AS) were asso
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f9053e5b30127d3eaade1d54ab61b5d3
https://doi.org/10.1136/ard.62.8.775
https://doi.org/10.1136/ard.62.8.775
Publikováno v:
South African Journal of Obstetrics and Gynaecology, Vol 21, Iss 2, Pp 52-53 (2015)
Cornelia de Lange syndrome (CdLS) is a rare genetic disorder of unknown causation, associated with multiple congenital anomalies. Prenatal genetic diagnosis is possible, and the syndrome can occur in subsequent pregnancies of families with affected c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::578a87a7b1cb6a72eaac97d76989f947
https://doi.org/10.7196/sajog.890
https://doi.org/10.7196/sajog.890
Autor:
Ayşegül Ozantürk, Jan D Marshall, Gayle B Collin, Selma Düzenli, Robert P Marshall, Şükrü Candan, Tülay Tos, İhsan Esen, Mustafa Taşkesen, Atilla Çayır, Şükrü Öztürk, İhsan Üstün, Esra Ataman, Emin Karaca, Taha Reşid Özdemir, İlknur Erol, Fehime Kara Eroğlu, Deniz Torun, Erhan Parıltay, Elif Yılmaz-Güleç, Ender Karaca, M Emre Atabek, Nursel Elçioğlu, İlhan Satman, Claes Möller, Jean Muller, Jürgen K Naggert, Rıza Köksal Özgül
Publikováno v:
Journal of Human Genetics. 60:51-51
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::792f21acfc6290ea05ea191dd8d866a6
https://doi.org/10.1038/jhg.2014.101
https://doi.org/10.1038/jhg.2014.101
Publikováno v:
International Journal of Case Reports and Images. 5:215
Introduction: Pentalogy of cantrell is a rare syndrome of unknown etiology characterized by multiple structural congenital anomalies. case report: We aimed to present an early diagnosed case of pentalogy of cantrell accompanied by craniorachischisis.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::839e50124d5f295ca01a27c493a5e15b
https://doi.org/10.5348/ijcri-2014-03-476-cr-7
https://doi.org/10.5348/ijcri-2014-03-476-cr-7
Autor:
Ozantürk, Ayşegül, Marshall, Jan D, Collin, Gayle B, Düzenli, Selma, Marshall, Robert P, Candan, Şükrü, Tos, Tülay, Esen, İhsan, Taşkesen, Mustafa, Çayır, Atilla, Öztürk, Şükrü, Üstün, İhsan, Ataman, Esra, Karaca, Emin, Özdemir, Taha Reşid, Erol, İlknur, Eroğlu, Fehime Kara, Torun, Deniz, Parıltay, Erhan, Yılmaz-Güleç, Elif
Publikováno v:
Journal of Human Genetics. Jan2015, Vol. 60 Issue 1, p51-51. 1p.