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Maigi Külm

Showing results (1-10 of 6) with videos related to

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The Journal of Molecular Diagnostics : JMD|March 27, 2007
Comprehensive arrayed primer extension array for the detection of 59 sequence variants in 15 conditions prevalent among the (Ashkenazi) Jewish populationIris Schrijver, Maigi Külm, Phyllis I Gardner, et al.
European Journal of Ophthalmology|July 14, 2015
Leber congenital amaurosis: first genotyped Hungarian patients and report of 2 novel mutations in the CRB1 and CEP290 genesRita Vámos, Maigi Külm, Viktoria Szabó, et al.
Investigative Ophthalmology & Visual Science|August 27, 2005
Genotyping microarray (disease chip) for Leber congenital amaurosis: detection of modifier allelesJana Zernant, Maigi Külm, Sharola Dharmaraj, et al.
Molecular Vision|July 9, 2011
Molecular epidemiology of Usher syndrome in ItalyDiego Vozzi, Anu Aaspõllu, Emmanouil Athanasakis, et al.
Investigative Ophthalmology & Visual Science|August 18, 2009
Microarray-based mutation analysis of 183 Spanish families with Usher syndromeTeresa Jaijo, Elena Aller, Gema García-García, et al.
Journal of Medical Genetics|September 12, 2006
Development of a genotyping microarray for Usher syndromeFrans P M Cremers, William J Kimberling, Maigi Külm, et al.
Pageof 1

Showing results (1-10 of 6) with videos related to

Sort By:
Pageof 1
The Journal of Molecular Diagnostics : JMD|March 27, 2007
Comprehensive arrayed primer extension array for the detection of 59 sequence variants in 15 conditions prevalent among the (Ashkenazi) Jewish populationIris Schrijver, Maigi Külm, Phyllis I Gardner, et al.
European Journal of Ophthalmology|July 14, 2015
Leber congenital amaurosis: first genotyped Hungarian patients and report of 2 novel mutations in the CRB1 and CEP290 genesRita Vámos, Maigi Külm, Viktoria Szabó, et al.
Investigative Ophthalmology & Visual Science|August 27, 2005
Genotyping microarray (disease chip) for Leber congenital amaurosis: detection of modifier allelesJana Zernant, Maigi Külm, Sharola Dharmaraj, et al.
Molecular Vision|July 9, 2011
Molecular epidemiology of Usher syndrome in ItalyDiego Vozzi, Anu Aaspõllu, Emmanouil Athanasakis, et al.
Investigative Ophthalmology & Visual Science|August 18, 2009
Microarray-based mutation analysis of 183 Spanish families with Usher syndromeTeresa Jaijo, Elena Aller, Gema García-García, et al.
Journal of Medical Genetics|September 12, 2006
Development of a genotyping microarray for Usher syndromeFrans P M Cremers, William J Kimberling, Maigi Külm, et al.
Pageof 1