Zobrazeno 1 - 10
of 264
pro vyhledávání: '"Pinar, T."'
Publikováno v:
Community Genetics, 2005 Jan 01. 8(1), 44-47.
Externí odkaz:
https://www.jstor.org/stable/26679446
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America, 1976 Nov 01. 73(11), 4110-4114.
Externí odkaz:
https://www.jstor.org/stable/66464
Akademický článek
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Autor:
Zeng, Wen-Qi, Al-Yamani, Eiman, Acierno, James S., Slaugenhaupt, Susan, Gillis, Tammy, MacDonald, Marcy E., Ozand, Pinar T., Gusella, James F.
Publikováno v:
In The American Journal of Human Genetics 2005 77(1):16-26
Publikováno v:
In Clinica Chimica Acta 2003 335(1):21-26
Autor:
Sakati Nadia, Al-Odaib Ali, Al-Habit Ola, Colak Dilek, Alshidi Tarfa A, AbuDheim Nada, Al-Dosari Naji, Al-Zahrani Jawaher, Meyer Brian, Ozand Pinar T, Kaya Namik
Publikováno v:
Molecular Cytogenetics, Vol 4, Iss 1, p 9 (2011)
Abstract Background Genomic imbalances of the 12q telomere are rare; only a few patients having 12q24.31-q24.33 deletions were reported. Interestingly none of these were mosaic. Although some attempts have been made to establish phenotype/genotype in
Externí odkaz:
https://doaj.org/article/7ed7c61239bb44c590e4a86801bd1ce2
Autor:
Ozand Pinar T, Goyns Malcolm H, Shoukri Mohamed M, Al-Qahtani Ahmed, Al-Bakheet Al-Bandary, Chishti Muhammad A, Colak Dilek, Quackenbush John, Park Ben H, Kaya Namik
Publikováno v:
Molecular Cancer, Vol 9, Iss 1, p 146 (2010)
Abstract Background Hepatocellular carcinoma (HCC) is the third-leading cause of cancer-related deaths worldwide. It is often diagnosed at an advanced stage, and hence typically has a poor prognosis. To identify distinct molecular mechanisms for earl
Externí odkaz:
https://doaj.org/article/09116b41c6be4ebca5c03f5ed759c810
Publikováno v:
In Pediatric Neurology 2000 22(1):44-47
Autor:
Dhaunsi, Gursev S.1,2 dhaunsig@hotmail.com, Ozand, Pinar T.2
Publikováno v:
Clinical & Experimental Pharmacology & Physiology. Jan/Feb2004, Vol. 31 Issue 1/2, p46-49. 4p.