Zobrazeno 1 - 10
of 88
pro vyhledávání: '"Ozge Ozer"'
Autor:
Alison Etukakpan, Nilhan Uzman, Ozge Ozer, Toyin Tofade, Silvana Nair Leite, Arinola Joda, Yahya Choonara, Chiluba Mwila, Lilian M. Azzopardi, Aukje K. Mantel-Teeuwisse, Mohammad Rahal, Rula Darwish, Beom-Jin Lee, Rajani Shakya, Paul J. Gallagher, Pierre Moreau, Luis Lourenço, Ross A. McKinnon, Ralph J. Altiere
Publikováno v:
Exploratory Research in Clinical and Social Pharmacy, Vol 9, Iss , Pp 100234- (2023)
Background: A needs-based approach is desirable for the transformation of pharmaceutical education, and to link pharmaceutical education with the health needs of populations and national priorities. There are varying levels of data in the literature
Externí odkaz:
https://doaj.org/article/efc0573f8743425ba25c3f9bf42cb9be
Publikováno v:
Journal of Inequalities and Applications, Vol 2020, Iss 1, Pp 1-15 (2020)
Abstract Marble, one of the metamorphic rock formation products, forms by undergoing different physical and chemical processes. The marble samples are tested under laboratory conditions to understand these processes. This study aims to find whether t
Externí odkaz:
https://doaj.org/article/1c935666f83e46c3b0721b49540ef193
Autor:
Altug Koc, Ozge Ozer Kaya, Berk Ozyilmaz, Yasar B. Kutbay, Ozgur Kirbiyik, Taha R. Ozdemir, Kadri M. Erdogan, Merve Saka Guvenc, Deniz C. Oztekin, Mehmet Ozeren, Halil G. Pala, Atalay Ekin, Cenk Gezer, Alkim G. Sahingoz Yildirim, Bahar Konuralp Atakul, Secil Kurtulmus, Ugur Turhan, Cuneyt E. Taner
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 7, Iss 7, Pp n/a-n/a (2019)
Abstract Background Next‐generation sequencing (NGS) and discovery of fetal cell‐free DNA (cfDNA) in the maternal circulation render possible prenatal screening for trisomy 21 (Down syndrome), trisomy 18, trisomy 13, and sex chromosome aneuploidi
Externí odkaz:
https://doaj.org/article/64aa45006b664fc4a1c3f66f8b9cc2f2
Publikováno v:
Çukurova Üniversitesi Tıp Fakültesi Dergisi, Vol 40, Iss 1, Pp 169-173 (2015)
Phelan-McDermid syndrome, also known as 22q13.3 deletion syndrome, is characterized by global developmental delay, absent or delayed speech, generalized hypotonia, and minor physical anomalies. The deletion typically involves the terminal band 22q13.
Externí odkaz:
https://doaj.org/article/5f993c9a596c4a26b452f433d2f1a53b
Publikováno v:
AIP Conference Proceedings; 2024, Vol. 3094 Issue 1, p1-4, 4p
Akademický článek
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Akademický článek
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K zobrazení výsledku je třeba se přihlásit.
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Publikováno v:
Minerals; Volume 13; Issue 6; Pages: 772
Red soil is formed by weathering due to the effect of bedrock and various fluids in subtropical and tropical climate zones. The major and trace element geochemistry of red soil are important for understanding its environmental conditions and interpre
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=multidiscipl::33467ca2938f1d50467d06d7c9fb58cb
Autor:
Kalkan Ahmet Toygar, Ozge Ozer, Ugur Toprak, Belgin Efe, Aysen Akalin, Kebapci Medine Nur, Goknur Yorulmaz
Publikováno v:
Endocrine Abstracts.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6d17d4f00fd242f1d669c4d6f38d0311
https://doi.org/10.1530/endoabs.90.p810
https://doi.org/10.1530/endoabs.90.p810
Autor:
Ozge Ozer, Kayer Merve Apaydin, Evrim Yilmaz, Kebapci Medine Nur, Aysen Akalin, Belgin Efe, Acikalin Mustafa Fuat, Goknur Yorulmaz
Publikováno v:
Endocrine Abstracts.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d957a6789464d95d2d5432ea14790c03
https://doi.org/10.1530/endoabs.90.p540
https://doi.org/10.1530/endoabs.90.p540