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Maria A Musarella

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

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Journal of Ophthalmology|November 5, 2010
Current concepts in the treatment of retinitis pigmentosaMaria A Musarella, Ian M Macdonald
Survey of Ophthalmology|March 5, 2004
Ocular genetics: current understandingIan M MacDonald, Mai Tran, Maria A Musarella
Journal of Pediatric Ophthalmology and Strabismus|October 14, 2004
Symmetrical bilateral lens colobomas in two brothersAshim Aggarwal, Abdel-Rahman El-Bash, Steven Inker, et al.
Molecular Vision|January 29, 2003
Mutation screening of patients with Leber Congenital Amaurosis or the enhanced S-Cone Syndrome reveals a lack of sequence variations in the NRL geneCeren Acar, Alan J Mears, Beverly M Yashar, et al.
American Journal of Human Genetics|May 7, 2002
A comprehensive mutation analysis of RP2 and RPGR in a North American cohort of families with X-linked retinitis pigmentosaDebra K Breuer, Beverly M Yashar, Elena Filippova, et al.
Investigative Ophthalmology & Visual Science|December 7, 2007
Identification of novel mutations in patients with Leber congenital amaurosis and juvenile RP by genome-wide homozygosity mapping with SNP microarraysAnneke I den Hollander, Irma Lopez, Suzanne Yzer, et al.
Pageof 1

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

Sort By:
Pageof 1
Journal of Ophthalmology|November 5, 2010
Current concepts in the treatment of retinitis pigmentosaMaria A Musarella, Ian M Macdonald
Survey of Ophthalmology|March 5, 2004
Ocular genetics: current understandingIan M MacDonald, Mai Tran, Maria A Musarella
Journal of Pediatric Ophthalmology and Strabismus|October 14, 2004
Symmetrical bilateral lens colobomas in two brothersAshim Aggarwal, Abdel-Rahman El-Bash, Steven Inker, et al.
Molecular Vision|January 29, 2003
Mutation screening of patients with Leber Congenital Amaurosis or the enhanced S-Cone Syndrome reveals a lack of sequence variations in the NRL geneCeren Acar, Alan J Mears, Beverly M Yashar, et al.
American Journal of Human Genetics|May 7, 2002
A comprehensive mutation analysis of RP2 and RPGR in a North American cohort of families with X-linked retinitis pigmentosaDebra K Breuer, Beverly M Yashar, Elena Filippova, et al.
Investigative Ophthalmology & Visual Science|December 7, 2007
Identification of novel mutations in patients with Leber congenital amaurosis and juvenile RP by genome-wide homozygosity mapping with SNP microarraysAnneke I den Hollander, Irma Lopez, Suzanne Yzer, et al.
Pageof 1