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George Kitsos

Showing results (31-40 of 35) with videos related to

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Molecular Cytogenetics|November 11, 2010
The use of array-CGH in a cohort of Greek children with developmental delayEmmanouil Manolakos, Annalisa Vetro, Konstantinos Kefalas, et al.
Clinical Ophthalmology (Auckland, N.Z.)|April 15, 2010
Primary open angle glaucoma due to T377M MYOC: Population mapping of a Greek founder mutation in Northwestern GreeceGeorge Kitsos, Zacharias Petrou, Maria Grigoriadou, et al.
Molecular Vision|April 10, 2007
Investigation of founder effects for the Thr377Met Myocilin mutation in glaucoma families from differing ethnic backgroundsAlex W Hewitt, John R Samples, R Rand Allingham, et al.
Investigative Ophthalmology & Visual Science|January 25, 2006
A large GLC1C Greek family with a myocilin T377M mutation: inheritance and phenotypic variabilityMichael B Petersen, George Kitsos, John R Samples, et al.
American Journal of Medical Genetics. Part A|January 20, 2007
A report on 10 new patients with heterozygous mutations in the COL11A1 gene and a review of genotype-phenotype correlations in type XI collagenopathiesMarja Majava, Kristien P Hoornaert, Deborah Bartholdi, et al.
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Showing results (31-40 of 35) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 35 results.
Molecular Cytogenetics|November 11, 2010
The use of array-CGH in a cohort of Greek children with developmental delayEmmanouil Manolakos, Annalisa Vetro, Konstantinos Kefalas, et al.
Clinical Ophthalmology (Auckland, N.Z.)|April 15, 2010
Primary open angle glaucoma due to T377M MYOC: Population mapping of a Greek founder mutation in Northwestern GreeceGeorge Kitsos, Zacharias Petrou, Maria Grigoriadou, et al.
Molecular Vision|April 10, 2007
Investigation of founder effects for the Thr377Met Myocilin mutation in glaucoma families from differing ethnic backgroundsAlex W Hewitt, John R Samples, R Rand Allingham, et al.
Investigative Ophthalmology & Visual Science|January 25, 2006
A large GLC1C Greek family with a myocilin T377M mutation: inheritance and phenotypic variabilityMichael B Petersen, George Kitsos, John R Samples, et al.
American Journal of Medical Genetics. Part A|January 20, 2007
A report on 10 new patients with heterozygous mutations in the COL11A1 gene and a review of genotype-phenotype correlations in type XI collagenopathiesMarja Majava, Kristien P Hoornaert, Deborah Bartholdi, et al.
Pageof 4