Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Nicola K Ragge

Showing results (1-10 of 34) with videos related to

Pageof 4
Sort By:
Molecular Vision|July 24, 2009
Molecular analysis of FOXC1 in subjects presenting with severe developmental eye anomaliesKulvinder Kaur, Nicola K Ragge, Jiannis Ragoussis
Clinical Dysmorphology|October 18, 2014
Branchio-oculo-facial syndrome: a three generational family with markedly variable phenotype including neonatal lethalityHannah L Titheradge, Chirag Patel, Nicola K Ragge
British Journal of Plastic Surgery|July 23, 2003
The surgical management of childhood orbito-temporal neurofibromatosisVickie Lee, Nicola K Ragge, J Richard O Collin
Ophthalmology|March 17, 2004
Orbitotemporal neurofibromatosis. Clinical features and surgical managementVickie Lee, Nicola K Ragge, J Richard O Collin
Molecular Vision|December 16, 2011
Parent-of-origin effects in SOX2 anophthalmia syndromeRobert J Osborne, Jennifer J Kurinczuk, Nicola K Ragge
Human Mutation|May 28, 2010
Bone morphogenetic protein 7 (BMP7) mutations are associated with variable ocular, brain, ear, palate, and skeletal anomaliesAlexander W Wyatt, Robert J Osborne, Helen Stewart, et al.
Human Genetics|February 15, 2019
Genetics of anophthalmia and microphthalmia. Part 1: Non-syndromic anophthalmia/microphthalmiaJ Plaisancié, F Ceroni, R Holt, et al.
American Journal of Ophthalmology|February 5, 2003
Ocular tilt reaction due to a mesencephalic lesion in juvenile polyarteritis nodosaNicola K Ragge, Christopher M Harris, Michael J Dillon, et al.
The European Journal of Neuroscience|July 6, 2006
Early midline interactions are important in mouse optic chiasm formation but are not critical in man: a significant distinction between man and mouseMagella M Neveu, Graham E Holder, Nicola K Ragge, et al.
BMC Genetics|November 13, 2010
Genetic defects of GDF6 in the zebrafish out of sight mutant and in human eye developmental anomaliesAnneke I den Hollander, Janisha Biyanwila, Peter Kovach, et al.
Pageof 4

Showing results (1-10 of 34) with videos related to

Sort By:
Pageof 4
Molecular Vision|July 24, 2009
Molecular analysis of FOXC1 in subjects presenting with severe developmental eye anomaliesKulvinder Kaur, Nicola K Ragge, Jiannis Ragoussis
Clinical Dysmorphology|October 18, 2014
Branchio-oculo-facial syndrome: a three generational family with markedly variable phenotype including neonatal lethalityHannah L Titheradge, Chirag Patel, Nicola K Ragge
British Journal of Plastic Surgery|July 23, 2003
The surgical management of childhood orbito-temporal neurofibromatosisVickie Lee, Nicola K Ragge, J Richard O Collin
Ophthalmology|March 17, 2004
Orbitotemporal neurofibromatosis. Clinical features and surgical managementVickie Lee, Nicola K Ragge, J Richard O Collin
Molecular Vision|December 16, 2011
Parent-of-origin effects in SOX2 anophthalmia syndromeRobert J Osborne, Jennifer J Kurinczuk, Nicola K Ragge
Human Mutation|May 28, 2010
Bone morphogenetic protein 7 (BMP7) mutations are associated with variable ocular, brain, ear, palate, and skeletal anomaliesAlexander W Wyatt, Robert J Osborne, Helen Stewart, et al.
Human Genetics|February 15, 2019
Genetics of anophthalmia and microphthalmia. Part 1: Non-syndromic anophthalmia/microphthalmiaJ Plaisancié, F Ceroni, R Holt, et al.
American Journal of Ophthalmology|February 5, 2003
Ocular tilt reaction due to a mesencephalic lesion in juvenile polyarteritis nodosaNicola K Ragge, Christopher M Harris, Michael J Dillon, et al.
The European Journal of Neuroscience|July 6, 2006
Early midline interactions are important in mouse optic chiasm formation but are not critical in man: a significant distinction between man and mouseMagella M Neveu, Graham E Holder, Nicola K Ragge, et al.
BMC Genetics|November 13, 2010
Genetic defects of GDF6 in the zebrafish out of sight mutant and in human eye developmental anomaliesAnneke I den Hollander, Janisha Biyanwila, Peter Kovach, et al.
Pageof 4