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Gail Billingsley

Showing results (1-10 of 17) with videos related to

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Ophthalmic Genetics|April 6, 2011
BBS mutational analysis: a strategic approachGail Billingsley, Catherine Deveault, Elise Héon
Ophthalmic Genetics|May 26, 2012
Mutational analysis of SDCCAG8 in Bardet-Biedl syndrome patients with renal involvement and absent polydactylyGail Billingsley, Ajoy Vincent, Catherine Deveault, et al.
Ophthalmic Genetics|January 28, 2011
Oligocone trichromacy is part of the spectrum of CNGA3-related cone system disordersAjoy Vincent, Tom Wright, Gail Billingsley, et al.
Acta Ophthalmologica|May 13, 2009
Clinical phenotype of posterior polymorphous corneal dystrophy in a family with a novel ZEB1 mutationDan Q Nguyen, Mohsen Hosseini, Gail Billingsley, et al.
Human Mutation|April 30, 2009
BBS7 and TTC8 (BBS8) mutations play a minor role in the mutational load of Bardet-Biedl syndrome in a multiethnic populationJenea Bin, Jagadeesan Madhavan, Walter Ferrini, et al.
Ophthalmic Research|March 21, 2003
Further genetic heterogeneity for autosomal dominant human sutural cataractsNorman Klopp, Elise Héon, Gail Billingsley, et al.
Molecular Vision|June 1, 2006
Further support of the role of CYP1B1 in patients with Peters anomalyAndrea Vincent, Gail Billingsley, Megan Priston, et al.
American Journal of Human Genetics|January 5, 2002
Digenic inheritance of early-onset glaucoma: CYP1B1, a potential modifier geneAndrea L Vincent, Gail Billingsley, Yvonne Buys, et al.
Molecular Genetics & Genomic Medicine|November 29, 2018
Retrotransposon insertion as a novel mutational event in Bardet-Biedl syndromeErika Tavares, Chen Yu Tang, Anjali Vig, et al.
Molecular Vision|August 20, 2005
CRYBB1 mutation associated with congenital cataract and microcorneaColin E Willoughby, Ayad Shafiq, Walter Ferrini, et al.
Pageof 2

Showing results (1-10 of 17) with videos related to

Sort By:
Pageof 2
Ophthalmic Genetics|April 6, 2011
BBS mutational analysis: a strategic approachGail Billingsley, Catherine Deveault, Elise Héon
Ophthalmic Genetics|May 26, 2012
Mutational analysis of SDCCAG8 in Bardet-Biedl syndrome patients with renal involvement and absent polydactylyGail Billingsley, Ajoy Vincent, Catherine Deveault, et al.
Ophthalmic Genetics|January 28, 2011
Oligocone trichromacy is part of the spectrum of CNGA3-related cone system disordersAjoy Vincent, Tom Wright, Gail Billingsley, et al.
Acta Ophthalmologica|May 13, 2009
Clinical phenotype of posterior polymorphous corneal dystrophy in a family with a novel ZEB1 mutationDan Q Nguyen, Mohsen Hosseini, Gail Billingsley, et al.
Human Mutation|April 30, 2009
BBS7 and TTC8 (BBS8) mutations play a minor role in the mutational load of Bardet-Biedl syndrome in a multiethnic populationJenea Bin, Jagadeesan Madhavan, Walter Ferrini, et al.
Ophthalmic Research|March 21, 2003
Further genetic heterogeneity for autosomal dominant human sutural cataractsNorman Klopp, Elise Héon, Gail Billingsley, et al.
Molecular Vision|June 1, 2006
Further support of the role of CYP1B1 in patients with Peters anomalyAndrea Vincent, Gail Billingsley, Megan Priston, et al.
American Journal of Human Genetics|January 5, 2002
Digenic inheritance of early-onset glaucoma: CYP1B1, a potential modifier geneAndrea L Vincent, Gail Billingsley, Yvonne Buys, et al.
Molecular Genetics & Genomic Medicine|November 29, 2018
Retrotransposon insertion as a novel mutational event in Bardet-Biedl syndromeErika Tavares, Chen Yu Tang, Anjali Vig, et al.
Molecular Vision|August 20, 2005
CRYBB1 mutation associated with congenital cataract and microcorneaColin E Willoughby, Ayad Shafiq, Walter Ferrini, et al.
Pageof 2