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Allan Richards

Showing results (1-10 of 14) with videos related to

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American Journal of Ophthalmology|September 5, 2002
A frame shift mutation in a tissue-specific alternatively spliced exon of collagen 2A1 in Wagner's vitreoretinal degenerationMartin Snead, Allan Richards
Journal of Paediatrics and Child Health|October 26, 2012
Clinical phenotypes associated with type II collagen mutationsInderraj Hanspal, Annie McNinch, Allan Richards, et al.
Ophthalmic Genetics|May 31, 2017
Type I membranous anomaly in Stickler syndromePhilip Alexander, Arabella Poulson, Annie McNinch, et al.
Lancet (London, England)|July 13, 2017
Retinal detachment in severe myopiaIoannis Dragoumis, Allan Richards, Philip Alexander, et al.
Journal of AAPOS : the Official Publication of the American Association for Pediatric Ophthalmology and Strabismus|April 16, 2025
Myopia progression in children with Stickler syndrome: a longitudinal cohort studyNisha Nixon, Kelly H Cheng, Allan Richards, et al.
American Journal of Medical Genetics. Part A|May 16, 2019
Homozygous Type IX collagen variants (COL9A1, COL9A2, and COL9A3) causing recessive Stickler syndrome-Expanding the phenotypeThomas R W Nixon, Philip Alexander, Allan Richards, et al.
BMC Medical Genetics|April 30, 2013
Deletions within COL11A1 in Type 2 stickler syndrome detected by multiplex ligation-dependent probe amplification (MLPA)Raymon Vijzelaar, Sarah Waller, Abdellatif Errami, et al.
European Archives of Oto-Rhino-Laryngology : Official Journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : Affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery|September 9, 2020
Auditory dysfunction in type 2 Stickler SyndromePhilip Alexander, Philip Gomersall, Jack Stancel-Lewis, et al.
European Journal of Human Genetics : EJHG|December 21, 2018
Bone morphogenetic protein 4 (BMP4) loss-of-function variant associated with autosomal dominant Stickler syndrome and renal dysplasiaThomas R W Nixon, Allan Richards, Laura K Towns, et al.
The New England Journal of Medicine|April 5, 2023
Cambridge Prophylactic Protocol, Retinal Detachment, and Stickler SyndromePhilip Alexander, Gregory S Fincham, Senjah Brown, et al.
Pageof 2

Showing results (1-10 of 14) with videos related to

Sort By:
Pageof 2
American Journal of Ophthalmology|September 5, 2002
A frame shift mutation in a tissue-specific alternatively spliced exon of collagen 2A1 in Wagner's vitreoretinal degenerationMartin Snead, Allan Richards
Journal of Paediatrics and Child Health|October 26, 2012
Clinical phenotypes associated with type II collagen mutationsInderraj Hanspal, Annie McNinch, Allan Richards, et al.
Ophthalmic Genetics|May 31, 2017
Type I membranous anomaly in Stickler syndromePhilip Alexander, Arabella Poulson, Annie McNinch, et al.
Lancet (London, England)|July 13, 2017
Retinal detachment in severe myopiaIoannis Dragoumis, Allan Richards, Philip Alexander, et al.
Journal of AAPOS : the Official Publication of the American Association for Pediatric Ophthalmology and Strabismus|April 16, 2025
Myopia progression in children with Stickler syndrome: a longitudinal cohort studyNisha Nixon, Kelly H Cheng, Allan Richards, et al.
American Journal of Medical Genetics. Part A|May 16, 2019
Homozygous Type IX collagen variants (COL9A1, COL9A2, and COL9A3) causing recessive Stickler syndrome-Expanding the phenotypeThomas R W Nixon, Philip Alexander, Allan Richards, et al.
BMC Medical Genetics|April 30, 2013
Deletions within COL11A1 in Type 2 stickler syndrome detected by multiplex ligation-dependent probe amplification (MLPA)Raymon Vijzelaar, Sarah Waller, Abdellatif Errami, et al.
European Archives of Oto-Rhino-Laryngology : Official Journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : Affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery|September 9, 2020
Auditory dysfunction in type 2 Stickler SyndromePhilip Alexander, Philip Gomersall, Jack Stancel-Lewis, et al.
European Journal of Human Genetics : EJHG|December 21, 2018
Bone morphogenetic protein 4 (BMP4) loss-of-function variant associated with autosomal dominant Stickler syndrome and renal dysplasiaThomas R W Nixon, Allan Richards, Laura K Towns, et al.
The New England Journal of Medicine|April 5, 2023
Cambridge Prophylactic Protocol, Retinal Detachment, and Stickler SyndromePhilip Alexander, Gregory S Fincham, Senjah Brown, et al.
Pageof 2