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Anan H Abbasi

Showing results (1-10 of 8) with videos related to

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Harefuah|July 25, 2009
[Ophthalmology in the Holy Land]Anan H Abbasi, Hanna J Garzozi
Harefuah|August 13, 2008
[Ophthalmology in the Middle East from antiquity to the twentieth century]Anan H Abbasi, Hanna J Garzozi
The Israel Medical Association Journal : IMAJ|December 19, 2007
Kidney-ear axisAnan H Abbasi, Rawi Ramadan, Aaron Hoffman, et al.
Molecular Vision|April 25, 2008
A novel splice-site mutation of TULP1 underlies severe early-onset retinitis pigmentosa in a consanguineous Israeli Muslim Arab familyAnan H Abbasi, Hanna J Garzozi, Tamar Ben-Yosef
Investigative Ophthalmology & Visual Science|December 7, 2007
A common founder mutation of CERKL underlies autosomal recessive retinal degeneration with early macular involvement among Yemenite JewsNoa Auslender, Dror Sharon, Anan H Abbasi, et al.
American Journal of Medical Genetics. Part A|January 14, 2009
Genetic heterogeneity in two consanguineous families segregating early onset retinal degeneration: the pitfalls of homozygosity mappingLiat Benayoun, Ronen Spiegel, Noa Auslender, et al.
American Journal of Human Genetics|April 20, 2010
Mutations in C2ORF71 cause autosomal-recessive retinitis pigmentosaRob W J Collin, Christine Safieh, Karin W Littink, et al.
Human Mutation|August 29, 2019
A nationwide genetic analysis of inherited retinal diseases in Israel as assessed by the Israeli inherited retinal disease consortium (IIRDC)Dror Sharon, Tamar Ben-Yosef, Nitza Goldenberg-Cohen, et al.
Pageof 1

Showing results (1-10 of 8) with videos related to

Sort By:
Pageof 1
Harefuah|July 25, 2009
[Ophthalmology in the Holy Land]Anan H Abbasi, Hanna J Garzozi
Harefuah|August 13, 2008
[Ophthalmology in the Middle East from antiquity to the twentieth century]Anan H Abbasi, Hanna J Garzozi
The Israel Medical Association Journal : IMAJ|December 19, 2007
Kidney-ear axisAnan H Abbasi, Rawi Ramadan, Aaron Hoffman, et al.
Molecular Vision|April 25, 2008
A novel splice-site mutation of TULP1 underlies severe early-onset retinitis pigmentosa in a consanguineous Israeli Muslim Arab familyAnan H Abbasi, Hanna J Garzozi, Tamar Ben-Yosef
Investigative Ophthalmology & Visual Science|December 7, 2007
A common founder mutation of CERKL underlies autosomal recessive retinal degeneration with early macular involvement among Yemenite JewsNoa Auslender, Dror Sharon, Anan H Abbasi, et al.
American Journal of Medical Genetics. Part A|January 14, 2009
Genetic heterogeneity in two consanguineous families segregating early onset retinal degeneration: the pitfalls of homozygosity mappingLiat Benayoun, Ronen Spiegel, Noa Auslender, et al.
American Journal of Human Genetics|April 20, 2010
Mutations in C2ORF71 cause autosomal-recessive retinitis pigmentosaRob W J Collin, Christine Safieh, Karin W Littink, et al.
Human Mutation|August 29, 2019
A nationwide genetic analysis of inherited retinal diseases in Israel as assessed by the Israeli inherited retinal disease consortium (IIRDC)Dror Sharon, Tamar Ben-Yosef, Nitza Goldenberg-Cohen, et al.
Pageof 1