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Showing results (811-820 of 1,250) with videos related to

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Molecular Vision|September 17, 2011
Autosomal dominant Best disease with an unusual electrooculographic light rise and risk of angle-closure glaucoma: a clinical and molecular genetic studySancy Low, Alice E Davidson, Graham E Holder, et al.
Ophthalmic Genetics|May 26, 2022
Variability of retinopathy consequent upon novel mutations in LAMA1Elena R Schiff, Nancy Aychoua, Savita Nutan, et al.
Ophthalmology|October 11, 2020
Autosomal Recessive Bestrophinopathy: Clinical Features, Natural History, and Genetic Findings in Preparation for Clinical TrialsGiuseppe Casalino, Kamron N Khan, Monica Armengol, et al.
BMJ Open|August 21, 2019
Feasibility study assessing equitable delivery of newborn pulse oximetry screening in New Zealand's midwifery-led maternity settingElza Cloete, Thomas L Gentles, Lesley A Dixon, et al.
Archives of General Psychiatry|May 16, 2001
Regional brain and ventricular volumes in Tourette syndromeB S Peterson, L Staib, L Scahill, et al.
Investigative Ophthalmology & Visual Science|November 1, 2011
Autosomal dominant retinitis pigmentosa with intrafamilial variability and incomplete penetrance in two families carrying mutations in PRPF8Cécilia G Maubaret, Veronika Vaclavik, Rajarshi Mukhopadhyay, et al.
Ophthalmology|February 6, 2018
Leber Congenital Amaurosis Associated with Mutations in CEP290, Clinical Phenotype, and Natural History in Preparation for Trials of Novel TherapiesLeo Sheck, Wayne I L Davies, Phillip Moradi, et al.
Ecology|January 14, 2009
Endogenous and exogenous control of ecosystem function: N cycling in headwater streamsH M Valett, S A Thomas, P J Mulholland, et al.
Molecular Genetics & Genomic Medicine|March 22, 2021
Panel-based genetic testing for inherited retinal disease screening 176 genesLeo H N Sheck, Simona D Esposti, Omar A Mahroo, et al.
Orphanet Journal of Rare Diseases|August 9, 2013
Screening for duplications, deletions and a common intronic mutation detects 35% of second mutations in patients with USH2A monoallelic mutations on Sanger sequencingHeather B Steele-Stallard, Polona Le Quesne Stabej, Eva Lenassi, et al.
Pageof 125

Showing results (811-820 of 1,250) with videos related to

Sort By:
Pageof 125
Molecular Vision|September 17, 2011
Autosomal dominant Best disease with an unusual electrooculographic light rise and risk of angle-closure glaucoma: a clinical and molecular genetic studySancy Low, Alice E Davidson, Graham E Holder, et al.
Ophthalmic Genetics|May 26, 2022
Variability of retinopathy consequent upon novel mutations in LAMA1Elena R Schiff, Nancy Aychoua, Savita Nutan, et al.
Ophthalmology|October 11, 2020
Autosomal Recessive Bestrophinopathy: Clinical Features, Natural History, and Genetic Findings in Preparation for Clinical TrialsGiuseppe Casalino, Kamron N Khan, Monica Armengol, et al.
BMJ Open|August 21, 2019
Feasibility study assessing equitable delivery of newborn pulse oximetry screening in New Zealand's midwifery-led maternity settingElza Cloete, Thomas L Gentles, Lesley A Dixon, et al.
Archives of General Psychiatry|May 16, 2001
Regional brain and ventricular volumes in Tourette syndromeB S Peterson, L Staib, L Scahill, et al.
Investigative Ophthalmology & Visual Science|November 1, 2011
Autosomal dominant retinitis pigmentosa with intrafamilial variability and incomplete penetrance in two families carrying mutations in PRPF8Cécilia G Maubaret, Veronika Vaclavik, Rajarshi Mukhopadhyay, et al.
Ophthalmology|February 6, 2018
Leber Congenital Amaurosis Associated with Mutations in CEP290, Clinical Phenotype, and Natural History in Preparation for Trials of Novel TherapiesLeo Sheck, Wayne I L Davies, Phillip Moradi, et al.
Ecology|January 14, 2009
Endogenous and exogenous control of ecosystem function: N cycling in headwater streamsH M Valett, S A Thomas, P J Mulholland, et al.
Molecular Genetics & Genomic Medicine|March 22, 2021
Panel-based genetic testing for inherited retinal disease screening 176 genesLeo H N Sheck, Simona D Esposti, Omar A Mahroo, et al.
Orphanet Journal of Rare Diseases|August 9, 2013
Screening for duplications, deletions and a common intronic mutation detects 35% of second mutations in patients with USH2A monoallelic mutations on Sanger sequencingHeather B Steele-Stallard, Polona Le Quesne Stabej, Eva Lenassi, et al.
Pageof 125