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Showing results (11-20 of 19) with videos related to

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Ophthalmic Plastic and Reconstructive Surgery|May 8, 2020
Rapid Rehabilitation With Skin-Muscle Sparing Orbital Exenteration: A Single-Center SeriesAnuradha Jayaprakasam, Kaveh Vahdani, Geoffrey E Rose, et al.
Transplantation|January 15, 2008
Innervation and secretory function of transplanted human submandibular salivary glandsGerd Geerling, John R Garrett, Katherine L Paterson, et al.
Human Mutation|September 11, 2008
Novel heterozygous OTX2 mutations and whole gene deletions in anophthalmia, microphthalmia and colobomaAlexander Wyatt, Preeti Bakrania, David J Bunyan, et al.
Nature Genetics|March 4, 2003
Mutations in SOX2 cause anophthalmiaJudy Fantes, Nicola K Ragge, Sally-Ann Lynch, et al.
Human Mutation|August 27, 2009
Seeing clearly: the dominant and recessive nature of FOXE3 in eye developmental anomaliesSibel Ugur Iseri, Robert J Osborne, Martin Farrall, et al.
Human Genetics|August 18, 2009
Reduced TFAP2A function causes variable optic fissure closure and retinal defects and sensitizes eye development to mutations in other morphogenetic regulatorsGaia Gestri, Robert J Osborne, Alexander W Wyatt, et al.
American Journal of Medical Genetics. Part A|April 7, 2005
SOX2 anophthalmia syndromeNicola K Ragge, Birgit Lorenz, Adele Schneider, et al.
American Journal of Human Genetics|February 7, 2008
Mutations in BMP4 cause eye, brain, and digit developmental anomalies: overlap between the BMP4 and hedgehog signaling pathwaysPreeti Bakrania, Maria Efthymiou, Johannes C Klein, et al.
American Journal of Human Genetics|April 23, 2005
Heterozygous mutations of OTX2 cause severe ocular malformationsNicola K Ragge, Alison G Brown, Charlotte M Poloschek, et al.
Pageof 2

Showing results (11-20 of 19) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 19 results.
Ophthalmic Plastic and Reconstructive Surgery|May 8, 2020
Rapid Rehabilitation With Skin-Muscle Sparing Orbital Exenteration: A Single-Center SeriesAnuradha Jayaprakasam, Kaveh Vahdani, Geoffrey E Rose, et al.
Transplantation|January 15, 2008
Innervation and secretory function of transplanted human submandibular salivary glandsGerd Geerling, John R Garrett, Katherine L Paterson, et al.
Human Mutation|September 11, 2008
Novel heterozygous OTX2 mutations and whole gene deletions in anophthalmia, microphthalmia and colobomaAlexander Wyatt, Preeti Bakrania, David J Bunyan, et al.
Nature Genetics|March 4, 2003
Mutations in SOX2 cause anophthalmiaJudy Fantes, Nicola K Ragge, Sally-Ann Lynch, et al.
Human Mutation|August 27, 2009
Seeing clearly: the dominant and recessive nature of FOXE3 in eye developmental anomaliesSibel Ugur Iseri, Robert J Osborne, Martin Farrall, et al.
Human Genetics|August 18, 2009
Reduced TFAP2A function causes variable optic fissure closure and retinal defects and sensitizes eye development to mutations in other morphogenetic regulatorsGaia Gestri, Robert J Osborne, Alexander W Wyatt, et al.
American Journal of Medical Genetics. Part A|April 7, 2005
SOX2 anophthalmia syndromeNicola K Ragge, Birgit Lorenz, Adele Schneider, et al.
American Journal of Human Genetics|February 7, 2008
Mutations in BMP4 cause eye, brain, and digit developmental anomalies: overlap between the BMP4 and hedgehog signaling pathwaysPreeti Bakrania, Maria Efthymiou, Johannes C Klein, et al.
American Journal of Human Genetics|April 23, 2005
Heterozygous mutations of OTX2 cause severe ocular malformationsNicola K Ragge, Alison G Brown, Charlotte M Poloschek, et al.
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