Zobrazeno 1 - 10
of 121
pro vyhledávání: '"Kokotas Haris"'
Autor:
Papadopoulou Anna, Kokotas Haris, Merou Konstantina, Kitsos George, Sofocleus Christalena, Leze Eleni, Kefalas Konstantinos, Vetro Annalisa, Sarri Catherine, Manolakos Emmanouil, Attilakos Achilleas, Petersen Michael B, Kitsiou-Tzeli Sofia
Publikováno v:
Molecular Cytogenetics, Vol 4, Iss 1, p 11 (2011)
Externí odkaz:
https://doaj.org/article/51e5c09cd6db4c02bd9c03250992f6c3
Autor:
Kokotas Haris, Orru Sandro, Mihalatos Markos, Weise Anja, Neroutsou Rozita, Thomaidis Loreta, Kosyakova Nadezda, Manolakos Emmanouil, Kitsos George, Liehr Thomas, Petersen Michael B
Publikováno v:
Molecular Cytogenetics, Vol 1, Iss 1, p 24 (2008)
Abstract We report on a 7 years and 4 months old Greek boy with mild microcephaly and dysmorphic facial features. He was a sociable child with maxillary hypoplasia, epicanthal folds, upslanting palpebral fissures with long eyelashes, and hyperteloris
Externí odkaz:
https://doaj.org/article/08d8a4f01e1742afa6f3a5e7431f6a13
Publikováno v:
In International Journal of Pediatric Otorhinolaryngology July 2012 76(7):969-971
Publikováno v:
In International Journal of Pediatric Otorhinolaryngology April 2012 76(4):549-551
Autor:
Kolaitis, Gerasimos, Papanikolaou, Katerina, Paliokosta, Elena, Tsiantis, John, Gyftodimou, Yolanda, Sarri, Catherine, Petersen, Michael, Kokotas, Haris
Publikováno v:
Advances in Mental Health and Learning Disabilities, 2009, Vol. 3, Issue 2, pp. 48-52.
Externí odkaz:
http://www.emeraldinsight.com/doi/10.1108/17530180200900021
Autor:
Kokotas, Haris, Grigoriadou, Maria, Yang, Li, Lodahl, Marianne, Rendtorff, Nanna Dahl, Gyftodimou, Yolanda, Korres, George S., Ferekidou, Elisabeth, Kandiloros, Dimitrios, Korres, Stavros, Tranebjærg, Lisbeth, Guan, Min-Xin, Petersen, Michael B.
Publikováno v:
In International Journal of Pediatric Otorhinolaryngology 2011 75(1):89-94
Autor:
Cordero, Jennifer Buenaventura, Williams, Robert W., Petersen, Michael B., Kokotas, Haris, Grigoriadou, Maria, Kitsos, George, Mandal, Nawajes A., Simpson, Claire L.
Publikováno v:
Cordero, J B, Williams, R W, Petersen, M B, Kokotas, H, Grigoriadou, M, Kitsos, G, Mandal, N A & Simpson, C L 2018, ' In silico functional analysis of genetic variants in chromosome 19 to identify disease-causing gene in a large Greek family with autosomal dominant macular dystrophy ', Investigative Ophthalmology & Visual Science, vol. 59, no. 9, 3141 . < https://iovs.arvojournals.org/article.aspx?articleid=2691083&resultClick=1 >
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::390b3b43adb392aea984a390ca37dc26
https://vbn.aau.dk/da/publications/1341b8e8-be68-47bd-a92e-10e1baeae75f
https://vbn.aau.dk/da/publications/1341b8e8-be68-47bd-a92e-10e1baeae75f
Autor:
Kokotas, Haris1, Grigoriadou, Maria1, Korres, George S.1, Ferekidou, Elisabeth1, Kandiloros, Dimitrios2, Korres, Stavros3, Petersen, Michael B.1
Publikováno v:
Disease Markers. 2011, Vol. 30 Issue 6, p283-289. 7p. 3 Charts.
Autor:
Kokotas, Haris1 hkokotas@yahoo.gr, Grigoriadou, Maria1, Korres, George S.1, Ferekidou, Elisabeth1, Giannoulia-Karantana, Aglaia2, Kandiloros, Dimitrios3, Korres, Stavros3, Petersen, Michael B.1
Publikováno v:
Journal of Human Genetics. May2010, Vol. 55 Issue 5, p265-269. 5p. 1 Chart.
Autor:
Kokotas, Haris1, Grigoriadou, Maria1, Mikkelsen, Margareta2, Giannoulia-Karantana, Aglaia1,3, Petersen, Michael B.1 mpetersen@ich.gr
Publikováno v:
Disease Markers. 2009, Vol. 27 Issue 6, p279-285. 7p. 1 Diagram, 1 Chart.