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Investigative Ophthalmology & Visual Science
|
April 16, 2010
Evidence of an asymmetrical endophenotype in congenital fibrosis of extraocular muscles type 3 resulting from TUBB3 mutations
Joseph L Demer, Robert A Clark, Max A Tischfield, et al.
Investigative Ophthalmology & Visual Science
|
January 2, 2007
Magnetic resonance imaging evidence for widespread orbital dysinnervation in dominant Duane's retraction syndrome linked to the DURS2 locus
Joseph L Demer, Robert A Clark, Key-Hwan Lim, et al.
Journal of Visualized Experiments : Jove
|
August 6, 2019
Ex Vivo Oculomotor Slice Culture from Embryonic GFP-Expressing Mice for Time-Lapse Imaging of Oculomotor Nerve Outgrowth
Mary C Whitman, Jessica L Bell, Elaine H Nguyen, et al.
Journal of AAPOS : the Official Publication of the American Association for Pediatric Ophthalmology and Strabismus
|
June 23, 2009
Clinical features associated with an I126M alpha2-chimaerin mutation in a family with autosomal-dominant Duane retraction syndrome
Claudia E Murillo-Correa, Veronica Kon-Jara, Elizabeth C Engle, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)
|
May 11, 2011
Two novel CHN1 mutations in 2 families with Duane retraction syndrome
Wai-Man Chan, Noriko Miyake, Lily Zhu-Tam, et al.
Journal of AAPOS : the Official Publication of the American Association for Pediatric Ophthalmology and Strabismus
|
May 6, 2008
Magnetic resonance imaging of the endophenotype of a novel familial Möbius-like syndrome
Sean Dumars, Caroline Andrews, Wai-Man Chan, et al.
Gene Expression Patterns : GEP
|
April 3, 2012
Spatiotemporal expression pattern of KIF21A during normal embryonic development and in congenital fibrosis of the extraocular muscles type 1 (CFEOM1)
Jigar Desai, Marie Pia Rogines Velo, Koki Yamada, et al.
Journal of Visualized Experiments : Jove
|
December 3, 2019
Isolation and Culture of Oculomotor, Trochlear, and Spinal Motor Neurons from Prenatal Islmn:GFP Transgenic Mice
Ryosuke Fujiki, Joun Y Lee, Julie A Jurgens, et al.
American Journal of Medical Genetics. Part A
|
March 11, 2006
HOXA1 mutations are not a common cause of Duane anomaly
Max A Tischfield, Wai-Man Chan, Jann-Frederik Grunert, et al.
American Journal of Medical Genetics. Part A
|
December 25, 2009
CHN1 mutations are not a common cause of sporadic Duane's retraction syndrome
Noriko Miyake, Caroline Andrews, Wen Fan, et al.
Page
of 13
Search research articles
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Showing results (31-40 of 125) with videos related to
Sort By:
Page
of 13
Investigative Ophthalmology & Visual Science
|
April 16, 2010
Evidence of an asymmetrical endophenotype in congenital fibrosis of extraocular muscles type 3 resulting from TUBB3 mutations
Joseph L Demer, Robert A Clark, Max A Tischfield, et al.
Investigative Ophthalmology & Visual Science
|
January 2, 2007
Magnetic resonance imaging evidence for widespread orbital dysinnervation in dominant Duane's retraction syndrome linked to the DURS2 locus
Joseph L Demer, Robert A Clark, Key-Hwan Lim, et al.
Journal of Visualized Experiments : Jove
|
August 6, 2019
Ex Vivo Oculomotor Slice Culture from Embryonic GFP-Expressing Mice for Time-Lapse Imaging of Oculomotor Nerve Outgrowth
Mary C Whitman, Jessica L Bell, Elaine H Nguyen, et al.
Journal of AAPOS : the Official Publication of the American Association for Pediatric Ophthalmology and Strabismus
|
June 23, 2009
Clinical features associated with an I126M alpha2-chimaerin mutation in a family with autosomal-dominant Duane retraction syndrome
Claudia E Murillo-Correa, Veronica Kon-Jara, Elizabeth C Engle, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)
|
May 11, 2011
Two novel CHN1 mutations in 2 families with Duane retraction syndrome
Wai-Man Chan, Noriko Miyake, Lily Zhu-Tam, et al.
Journal of AAPOS : the Official Publication of the American Association for Pediatric Ophthalmology and Strabismus
|
May 6, 2008
Magnetic resonance imaging of the endophenotype of a novel familial Möbius-like syndrome
Sean Dumars, Caroline Andrews, Wai-Man Chan, et al.
Gene Expression Patterns : GEP
|
April 3, 2012
Spatiotemporal expression pattern of KIF21A during normal embryonic development and in congenital fibrosis of the extraocular muscles type 1 (CFEOM1)
Jigar Desai, Marie Pia Rogines Velo, Koki Yamada, et al.
Journal of Visualized Experiments : Jove
|
December 3, 2019
Isolation and Culture of Oculomotor, Trochlear, and Spinal Motor Neurons from Prenatal Islmn:GFP Transgenic Mice
Ryosuke Fujiki, Joun Y Lee, Julie A Jurgens, et al.
American Journal of Medical Genetics. Part A
|
March 11, 2006
HOXA1 mutations are not a common cause of Duane anomaly
Max A Tischfield, Wai-Man Chan, Jann-Frederik Grunert, et al.
American Journal of Medical Genetics. Part A
|
December 25, 2009
CHN1 mutations are not a common cause of sporadic Duane's retraction syndrome
Noriko Miyake, Caroline Andrews, Wen Fan, et al.
Page
of 13