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Browsing by Author Shyr C

Showing results 1 to 5 of 5
Issue DateTitleAuthor(s)TypeМp-cat.
2015Defects in fatty acid amide hydrolase 2 in a male with neurologic and psychiatric symptoms and vertical gaze palsySirrs S; van Karnebeek C D; Peng X; Shyr C; Tarailo Graovac, Maja ; Mandal R; Testa D; Dubin D; Carbonetti G; Glynn S E;
Sayson B; Robinson W P; Han B; Wishart D; Ross C J; Wasserman W W; Hurwitz T A; Sinclair G; Kaczocha M;
Konferencijski rad
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2015FLAGS: candidate gene prioritization scheme based on frequently mutated genes in public exomesShyr C; Tarailo Graovac, Maja ; Gottlieb M; Lee J J Y; Van Karnebeek C; Wasserman W WKonferencijski rad
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2016Further Validation of the SIGMAR1 c.151+1G>T Mutation as Cause of Distal Hereditary Motor NeuropathyLee Jjy; Van Karnebeek Cdm; Drögemoller B; Shyr C; Tarailo Graovac, Maja ; Eydoux P; Ross Cj; Wasserman Ww; Björnson B; Wu JkNaučni članak
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2014Next Generation Approach to the Discovery of Treatable Intellectual Disability GenesTarailo Graovac, Maja ; Sinclair G; Stockler-Ipsiroglu S; Van Allen M; Rozmus J; Shyr C; Sayson B; Lafek M; Ross C J; W P;
Wasserman W W; Rossi A;
Konferencijski rad
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2015OMICS2TREATID: A collaborative approach to accelerate the discovery of rare neuro-metabolic diseasesTarailo Graovac, Maja ; Horvath G; Shyr C; Salvarinova R; Ye C; Wevers R A; Stockler S G; Wasserman W W; Van Karnebeek CKonferencijski rad
Mp kategorija će biti prikazana naknadno.