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Dikla Bandah

Showing results (1-10 of 17) with videos related to

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Archives of Ophthalmology (Chicago, Ill. : 1960)|March 11, 2009
The spectrum of retinal diseases caused by NR2E3 mutations in Israeli and Palestinian patientsDikla Bandah, Saul Merin, Munther Ashhab, et al.
Molecular Vision|March 13, 2008
A novel de novo PAX6 mutation in an Ashkenazi-Jewish family with aniridiaDikla Bandah, Ada Rosenmann, Anat Blumenfeld, et al.
Journal of Forensic Sciences|July 13, 2026
Nearly two decades on paper: DNA quantity and quality in buccal samples stored on FTA cardsYaara Levav-Cohen, Yifat Lamberti, Dikla Bandah, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|February 21, 2008
Microarray-based gene expression analysis during retinal maturation of albino ratsGil Ben-Shlomo, Ron Ofri, Dikla Bandah, et al.
Journal of Forensic Sciences|April 28, 2025
The power of STR discrimination: Two brothers with high-profile similarityDikla Bandah-Rozenfeld, Lev Voskoboinik, Ksenia Rashkovski, et al.
Investigative Ophthalmology & Visual Science|May 26, 2007
A complex expression pattern of Pax6 in the pigeon retinaDikla Bandah, Tomer Swissa, Gil Ben-Shlomo, et al.
Investigative Ophthalmology & Visual Science|March 2, 2013
Mutations in CRB1 are a relatively common cause of autosomal recessive early-onset retinal degeneration in the Israeli and Palestinian populationsAvigail Beryozkin, Lina Zelinger, Dikla Bandah-Rozenfeld, et al.
Molecular Vision|September 8, 2011
Enhanced S-cone function with preserved rod function: a new clinical phenotypeMichael Kinori, Eran Pras, Andrew Kolker, et al.
Investigative Ophthalmology & Visual Science|January 30, 2014
Identification of mutations causing inherited retinal degenerations in the israeli and palestinian populations using homozygosity mappingAvigail Beryozkin, Lina Zelinger, Dikla Bandah-Rozenfeld, et al.
Human Molecular Genetics|September 4, 2012
FAM161A, associated with retinitis pigmentosa, is a component of the cilia-basal body complex and interacts with proteins involved in ciliopathiesSilvio Alessandro Di Gioia, Stef J F Letteboer, Corinne Kostic, et al.
Pageof 2

Showing results (1-10 of 17) with videos related to

Sort By:
Pageof 2
Archives of Ophthalmology (Chicago, Ill. : 1960)|March 11, 2009
The spectrum of retinal diseases caused by NR2E3 mutations in Israeli and Palestinian patientsDikla Bandah, Saul Merin, Munther Ashhab, et al.
Molecular Vision|March 13, 2008
A novel de novo PAX6 mutation in an Ashkenazi-Jewish family with aniridiaDikla Bandah, Ada Rosenmann, Anat Blumenfeld, et al.
Journal of Forensic Sciences|July 13, 2026
Nearly two decades on paper: DNA quantity and quality in buccal samples stored on FTA cardsYaara Levav-Cohen, Yifat Lamberti, Dikla Bandah, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|February 21, 2008
Microarray-based gene expression analysis during retinal maturation of albino ratsGil Ben-Shlomo, Ron Ofri, Dikla Bandah, et al.
Journal of Forensic Sciences|April 28, 2025
The power of STR discrimination: Two brothers with high-profile similarityDikla Bandah-Rozenfeld, Lev Voskoboinik, Ksenia Rashkovski, et al.
Investigative Ophthalmology & Visual Science|May 26, 2007
A complex expression pattern of Pax6 in the pigeon retinaDikla Bandah, Tomer Swissa, Gil Ben-Shlomo, et al.
Investigative Ophthalmology & Visual Science|March 2, 2013
Mutations in CRB1 are a relatively common cause of autosomal recessive early-onset retinal degeneration in the Israeli and Palestinian populationsAvigail Beryozkin, Lina Zelinger, Dikla Bandah-Rozenfeld, et al.
Molecular Vision|September 8, 2011
Enhanced S-cone function with preserved rod function: a new clinical phenotypeMichael Kinori, Eran Pras, Andrew Kolker, et al.
Investigative Ophthalmology & Visual Science|January 30, 2014
Identification of mutations causing inherited retinal degenerations in the israeli and palestinian populations using homozygosity mappingAvigail Beryozkin, Lina Zelinger, Dikla Bandah-Rozenfeld, et al.
Human Molecular Genetics|September 4, 2012
FAM161A, associated with retinitis pigmentosa, is a component of the cilia-basal body complex and interacts with proteins involved in ciliopathiesSilvio Alessandro Di Gioia, Stef J F Letteboer, Corinne Kostic, et al.
Pageof 2