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The British Journal of Ophthalmology
|
July 15, 2019
Congenital monocular elevation deficiency associated with a novel <i>TUBB3</i> gene variant
Mervyn G Thomas, Gail D E Maconachie, Cris S Constantinescu, et al.
Muscle & Nerve
|
January 3, 2021
Differentiating Moebius syndrome and other congenital facial weakness disorders with electrodiagnostic studies
Tanya Lehky, Reversa Joseph, Camilo Toro, et al.
American Journal of Human Genetics
|
June 12, 2018
Recessive MYF5 Mutations Cause External Ophthalmoplegia, Rib, and Vertebral Anomalies
Silvio Alessandro Di Gioia, Sherin Shaaban, Beyhan Tüysüz, et al.
Developmental Cell
|
August 29, 2017
Cerebral Vein Malformations Result from Loss of Twist1 Expression and BMP Signaling from Skull Progenitor Cells and Dura
Max A Tischfield, Caroline D Robson, Nicole M Gilette, et al.
Nature Genetics
|
September 13, 2005
Homozygous HOXA1 mutations disrupt human brainstem, inner ear, cardiovascular and cognitive development
Max A Tischfield, Thomas M Bosley, Mustafa A M Salih, et al.
Brain Communications
|
April 25, 2020
Brain phenotyping in Moebius syndrome and other congenital facial weakness disorders by diffusion MRI morphometry
Neda Sadeghi, Elizabeth Hutchinson, Carol Van Ryzin, et al.
Elife
|
June 4, 2019
Stem cell-derived cranial and spinal motor neurons reveal proteostatic differences between ALS resistant and sensitive motor neurons
Disi An, Ryosuke Fujiki, Dylan E Iannitelli, et al.
International Journal of Molecular Sciences
|
April 3, 2021
Optic Nerve Head and Retinal Abnormalities Associated with Congenital Fibrosis of the Extraocular Muscles
Mervyn G Thomas, Gail D E Maconachie, Helen J Kuht, et al.
Journal of AAPOS : the Official Publication of the American Association for Pediatric Ophthalmology and Strabismus
|
January 14, 2024
The influence of orbital architecture on strabismus in craniosynostosis
Tonya C Lee, Evan Walker, Michelle A Ting, et al.
American Journal of Medical Genetics. Part A
|
December 8, 2015
Two unique TUBB3 mutations cause both CFEOM3 and malformations of cortical development
Mary C Whitman, Caroline Andrews, Wai-Man Chan, et al.
Page
of 13
Search research articles
Search
Showing results (71-80 of 125) with videos related to
Sort By:
Page
of 13
The British Journal of Ophthalmology
|
July 15, 2019
Congenital monocular elevation deficiency associated with a novel <i>TUBB3</i> gene variant
Mervyn G Thomas, Gail D E Maconachie, Cris S Constantinescu, et al.
Muscle & Nerve
|
January 3, 2021
Differentiating Moebius syndrome and other congenital facial weakness disorders with electrodiagnostic studies
Tanya Lehky, Reversa Joseph, Camilo Toro, et al.
American Journal of Human Genetics
|
June 12, 2018
Recessive MYF5 Mutations Cause External Ophthalmoplegia, Rib, and Vertebral Anomalies
Silvio Alessandro Di Gioia, Sherin Shaaban, Beyhan Tüysüz, et al.
Developmental Cell
|
August 29, 2017
Cerebral Vein Malformations Result from Loss of Twist1 Expression and BMP Signaling from Skull Progenitor Cells and Dura
Max A Tischfield, Caroline D Robson, Nicole M Gilette, et al.
Nature Genetics
|
September 13, 2005
Homozygous HOXA1 mutations disrupt human brainstem, inner ear, cardiovascular and cognitive development
Max A Tischfield, Thomas M Bosley, Mustafa A M Salih, et al.
Brain Communications
|
April 25, 2020
Brain phenotyping in Moebius syndrome and other congenital facial weakness disorders by diffusion MRI morphometry
Neda Sadeghi, Elizabeth Hutchinson, Carol Van Ryzin, et al.
Elife
|
June 4, 2019
Stem cell-derived cranial and spinal motor neurons reveal proteostatic differences between ALS resistant and sensitive motor neurons
Disi An, Ryosuke Fujiki, Dylan E Iannitelli, et al.
International Journal of Molecular Sciences
|
April 3, 2021
Optic Nerve Head and Retinal Abnormalities Associated with Congenital Fibrosis of the Extraocular Muscles
Mervyn G Thomas, Gail D E Maconachie, Helen J Kuht, et al.
Journal of AAPOS : the Official Publication of the American Association for Pediatric Ophthalmology and Strabismus
|
January 14, 2024
The influence of orbital architecture on strabismus in craniosynostosis
Tonya C Lee, Evan Walker, Michelle A Ting, et al.
American Journal of Medical Genetics. Part A
|
December 8, 2015
Two unique TUBB3 mutations cause both CFEOM3 and malformations of cortical development
Mary C Whitman, Caroline Andrews, Wai-Man Chan, et al.
Page
of 13