Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Ebru TUNÇEZ"'
Autor:
Serdal Baştuğ, Büşranur Çavdarlı, Aliye Baştuğ, İrfan Şencan, Ebru Tunçez, Esra Yakışık Çakır, Nizamettin Kemirtlek, Cihad Sakar, Deniz Erdem, Gülay Güleç Ceylan, Işıl Özkoçak Turan, Sümeyye Kazancıoğlu, Hürrem Bodur
Publikováno v:
Anatolian Journal of Cardiology, Vol 26, Iss 2, Pp 133-140 (2022)
Objective: The impact of the coronavirus disease 2019 (COVID-19) pandemic has been unceasingly ongoing worldwide. Recent bioinformatics analysis and epidemiologic studies have highlighted that the functional polymorphisms on the angiotensin convertin
Externí odkaz:
https://doaj.org/article/59014e3b4f684787be908e1dd606900a
Publikováno v:
Hematology, Transfusion and Cell Therapy, Vol 43, Iss , Pp S25-S26 (2021)
Objective: Intrachromosomal amplification of chromosome 21 (iAMP21) is defined as the presence of three or more RUNX1 signals on a single chromosome, or a total of five or more RUNX1 signals per cell. It occurs in 2% of pediatric B-cell acute lymphob
Externí odkaz:
https://doaj.org/article/c9c61f0e417f4c0d8ab14cdbfe8bc9c8
Publikováno v:
Hematology, Transfusion and Cell Therapy, Vol 43, Iss, Pp S25-S26 (2021)
Objective Intrachromosomal amplification of chromosome 21 (iAMP21) is defined as the presence of three or more RUNX1 signals on a single chromosome, or a total of five or more RUNX1 signals per cell. It occurs in 2% of pediatric B-cell acute lymphobl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fb3d5c10197039365b7db07a15f198fb
https://doi.org/10.1016/j.htct.2021.10.994
https://doi.org/10.1016/j.htct.2021.10.994
Publikováno v:
Pamukkale Medical Journal.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::94ee7a069d1c093637924dbd9ac33d04
https://doi.org/10.31362/patd.757219
https://doi.org/10.31362/patd.757219
Publikováno v:
Turkiye Klinikleri Journal of Ophthalmology. 26:293-296
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::394ab4b58c80ef214adeb8fdff5d4082
https://doi.org/10.5336/ophthal.2016-50074
https://doi.org/10.5336/ophthal.2016-50074
Publikováno v:
Family Practice and Palliative Care, Vol 6, Iss 3, Pp 105-110 (2021)
Introduction: Beta-thalassemia is an autosomal recessive disease that occurs as a result of a disorder in the (β-globin chains synthesis), and the gold standard method for diagnosis is genetic mutation analysis. It is important to know the distribut
Externí odkaz:
https://doaj.org/article/437d8b7833c54a58a56eda643bccc74b
Publikováno v:
Turkish Journal of Hematology, Vol 36, Iss 1, Pp 50-51 (2019)
Externí odkaz:
https://doaj.org/article/17f95913264b4bf1849338740be66ce9