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Haris Kokotas

Showing results (1-10 of 27) with videos related to

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Clinical Chemistry and Laboratory Medicine|December 24, 2010
Age-related macular degeneration: genetic and clinical findingsHaris Kokotas, Maria Grigoriadou, Michael B Petersen
International Journal of Pediatric Otorhinolaryngology|February 11, 2012
Compound heterozygosity of the novel c.292C>T (p.R98W) and the c.35delG GJB2 mutations in postlingual, non-syndromic, sensorineural deafnessMichael B Petersen, Maria Grigoriadou, John Economides, et al.
International Journal of Pediatric Otorhinolaryngology|April 10, 2012
The novel c.247_249delTTC (p.F83del) GJB2 mutation in a family with prelingual sensorineural deafnessMichael B Petersen, Maria Grigoriadou, Maria Koutroumpe, et al.
European Journal of Dermatology : EJD|January 24, 2012
Erythrokeratodermia variabilis: report of two cases and a novel missense variant in GJB4 encoding connexin 30.3Haris Kokotas, Konstantina Papagiannaki, Maria Grigoriadou, et al.
Disease Markers|January 16, 2010
Investigating the impact of the Down syndrome related common MTHFR 677C>T polymorphism in the Danish populationHaris Kokotas, Maria Grigoriadou, Margareta Mikkelsen, et al.
Genetic Testing and Molecular Biomarkers|January 12, 2010
Easy, rapid, and cost-effective methods for identifying carriers of recurrent GJB2 mutations causing nonsyndromic hearing impairment in the Greek populationHaris Kokotas, Maria Grigoriadou, Angeliki Hatzaki, et al.
Genetic Testing and Molecular Biomarkers|January 16, 2010
Hypothesizing an ancient Greek origin of the GJB2 35delG mutation: can science meet history?Haris Kokotas, Maria Grigoriadou, Manuela Villamar, et al.
Clinical Chemistry and Laboratory Medicine|June 30, 2012
Biomarkers in primary open angle glaucomaHaris Kokotas, Christos Kroupis, Dimitrios Chiras, et al.
Disease Markers|July 5, 2011
Detection of deafness-causing mutations in the Greek mitochondrial genomeHaris Kokotas, Maria Grigoriadou, George S Korres, et al.
Molecular Vision|November 9, 2011
A novel PIKFYVE mutation in fleck corneal dystrophyAndreas Kotoulas, Haris Kokotas, Konstantinos Kopsidas, et al.
Pageof 3

Showing results (1-10 of 27) with videos related to

Sort By:
Pageof 3
Clinical Chemistry and Laboratory Medicine|December 24, 2010
Age-related macular degeneration: genetic and clinical findingsHaris Kokotas, Maria Grigoriadou, Michael B Petersen
International Journal of Pediatric Otorhinolaryngology|February 11, 2012
Compound heterozygosity of the novel c.292C>T (p.R98W) and the c.35delG GJB2 mutations in postlingual, non-syndromic, sensorineural deafnessMichael B Petersen, Maria Grigoriadou, John Economides, et al.
International Journal of Pediatric Otorhinolaryngology|April 10, 2012
The novel c.247_249delTTC (p.F83del) GJB2 mutation in a family with prelingual sensorineural deafnessMichael B Petersen, Maria Grigoriadou, Maria Koutroumpe, et al.
European Journal of Dermatology : EJD|January 24, 2012
Erythrokeratodermia variabilis: report of two cases and a novel missense variant in GJB4 encoding connexin 30.3Haris Kokotas, Konstantina Papagiannaki, Maria Grigoriadou, et al.
Disease Markers|January 16, 2010
Investigating the impact of the Down syndrome related common MTHFR 677C>T polymorphism in the Danish populationHaris Kokotas, Maria Grigoriadou, Margareta Mikkelsen, et al.
Genetic Testing and Molecular Biomarkers|January 12, 2010
Easy, rapid, and cost-effective methods for identifying carriers of recurrent GJB2 mutations causing nonsyndromic hearing impairment in the Greek populationHaris Kokotas, Maria Grigoriadou, Angeliki Hatzaki, et al.
Genetic Testing and Molecular Biomarkers|January 16, 2010
Hypothesizing an ancient Greek origin of the GJB2 35delG mutation: can science meet history?Haris Kokotas, Maria Grigoriadou, Manuela Villamar, et al.
Clinical Chemistry and Laboratory Medicine|June 30, 2012
Biomarkers in primary open angle glaucomaHaris Kokotas, Christos Kroupis, Dimitrios Chiras, et al.
Disease Markers|July 5, 2011
Detection of deafness-causing mutations in the Greek mitochondrial genomeHaris Kokotas, Maria Grigoriadou, George S Korres, et al.
Molecular Vision|November 9, 2011
A novel PIKFYVE mutation in fleck corneal dystrophyAndreas Kotoulas, Haris Kokotas, Konstantinos Kopsidas, et al.
Pageof 3