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Francoise Meire

Showing results (1-10 of 7) with videos related to

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Gait & Posture|August 31, 2010
Low vision affects dynamic stability of gaitAnn Hallemans, Els Ortibus, Francoise Meire, et al.
Research in Developmental Disabilities|October 12, 2011
Development of independent locomotion in children with a severe visual impairmentAnn Hallemans, Els Ortibus, Steven Truijen, et al.
Acta Ophthalmologica Scandinavica|November 7, 2006
The key role of electrophysiology in the diagnosis of visually impaired childrenMaria van Genderen, Frans Riemslag, Frank Jorritsma, et al.
Investigative Ophthalmology & Visual Science|November 24, 2004
A novel mutation in the ELOVL4 gene causes autosomal dominant Stargardt-like macular dystrophyAlessandra Maugeri, Francoise Meire, Carel B Hoyng, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 9, 2019
Recurrent heterozygous PAX6 missense variants cause severe bilateral microphthalmia via predictable effects on DNA-protein interactionKathleen A Williamson, H Nikki Hall, Liusaidh J Owen, et al.
American Journal of Human Genetics|February 14, 2012
Whole-exome sequencing identifies mutations in GPR179 leading to autosomal-recessive complete congenital stationary night blindnessIsabelle Audo, Kinga Bujakowska, Elise Orhan, et al.
Plos One|April 29, 2016
Genetic Analysis of 'PAX6-Negative' Individuals with Aniridia or Gillespie SyndromeMorad Ansari, Jacqueline Rainger, Isabel M Hanson, et al.
Pageof 1

Showing results (1-10 of 7) with videos related to

Sort By:
Pageof 1
Gait & Posture|August 31, 2010
Low vision affects dynamic stability of gaitAnn Hallemans, Els Ortibus, Francoise Meire, et al.
Research in Developmental Disabilities|October 12, 2011
Development of independent locomotion in children with a severe visual impairmentAnn Hallemans, Els Ortibus, Steven Truijen, et al.
Acta Ophthalmologica Scandinavica|November 7, 2006
The key role of electrophysiology in the diagnosis of visually impaired childrenMaria van Genderen, Frans Riemslag, Frank Jorritsma, et al.
Investigative Ophthalmology & Visual Science|November 24, 2004
A novel mutation in the ELOVL4 gene causes autosomal dominant Stargardt-like macular dystrophyAlessandra Maugeri, Francoise Meire, Carel B Hoyng, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 9, 2019
Recurrent heterozygous PAX6 missense variants cause severe bilateral microphthalmia via predictable effects on DNA-protein interactionKathleen A Williamson, H Nikki Hall, Liusaidh J Owen, et al.
American Journal of Human Genetics|February 14, 2012
Whole-exome sequencing identifies mutations in GPR179 leading to autosomal-recessive complete congenital stationary night blindnessIsabelle Audo, Kinga Bujakowska, Elise Orhan, et al.
Plos One|April 29, 2016
Genetic Analysis of 'PAX6-Negative' Individuals with Aniridia or Gillespie SyndromeMorad Ansari, Jacqueline Rainger, Isabel M Hanson, et al.
Pageof 1