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Linda M Reis

Showing results (1-10 of 59) with videos related to

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Human Genetics|September 7, 2018
Genetic landscape of isolated pediatric cataracts: extreme heterogeneity and variable inheritance patterns within genesLinda M Reis, Elena V Semina
Birth Defects Research. Part C, Embryo Today : Reviews|June 6, 2015
Conserved genetic pathways associated with microphthalmia, anophthalmia, and colobomaLinda M Reis, Elena V Semina
Current Opinion in Ophthalmology|July 7, 2011
Genetics of anterior segment dysgenesis disordersLinda M Reis, Elena V Semina
Pediatric Clinics of North America|July 29, 2006
Application of genetic approaches to ocular diseaseMark S Ruttum, Linda M Reis, Elena V Semina
Molecular Vision|June 19, 2014
Identification of a novel C-terminal extension mutation in EPHA2 in a family affected with congenital cataractLinda M Reis, Rebecca C Tyler, Elena V Semina
Human Genomics|March 29, 2025
Displacement of distant regulatory elements of FOXC1 as a potential human disease mechanismJesús-José Ferre-Fernández, Linda M Reis, Elena V Semina
Human Mutation|October 25, 2024
A <i>De Novo</i> Noncoding <i>RARB</i> Variant Associated with Complex Microphthalmia Alters a Putative Regulatory ElementMaria R Replogle, Samuel Thompson, Linda M Reis, et al.
Progress in Retinal and Eye Research|August 3, 2024
Congenital anterior segment ocular disorders: Genotype-phenotype correlations and emerging novel mechanismsLinda M Reis, Sarah E Seese, Deborah Costakos, et al.
Journal of Genetic Counseling|February 6, 2007
Spiritual assessment in genetic counselingLinda M Reis, Robert Baumiller, William Scrivener, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|June 30, 2015
EFTUD2 deficiency in vertebrates: Identification of a novel human mutation and generation of a zebrafish modelBrett Deml, Linda M Reis, Sanaa Muheisen, et al.
Pageof 6

Showing results (1-10 of 59) with videos related to

Sort By:
Pageof 6
Human Genetics|September 7, 2018
Genetic landscape of isolated pediatric cataracts: extreme heterogeneity and variable inheritance patterns within genesLinda M Reis, Elena V Semina
Birth Defects Research. Part C, Embryo Today : Reviews|June 6, 2015
Conserved genetic pathways associated with microphthalmia, anophthalmia, and colobomaLinda M Reis, Elena V Semina
Current Opinion in Ophthalmology|July 7, 2011
Genetics of anterior segment dysgenesis disordersLinda M Reis, Elena V Semina
Pediatric Clinics of North America|July 29, 2006
Application of genetic approaches to ocular diseaseMark S Ruttum, Linda M Reis, Elena V Semina
Molecular Vision|June 19, 2014
Identification of a novel C-terminal extension mutation in EPHA2 in a family affected with congenital cataractLinda M Reis, Rebecca C Tyler, Elena V Semina
Human Genomics|March 29, 2025
Displacement of distant regulatory elements of FOXC1 as a potential human disease mechanismJesús-José Ferre-Fernández, Linda M Reis, Elena V Semina
Human Mutation|October 25, 2024
A <i>De Novo</i> Noncoding <i>RARB</i> Variant Associated with Complex Microphthalmia Alters a Putative Regulatory ElementMaria R Replogle, Samuel Thompson, Linda M Reis, et al.
Progress in Retinal and Eye Research|August 3, 2024
Congenital anterior segment ocular disorders: Genotype-phenotype correlations and emerging novel mechanismsLinda M Reis, Sarah E Seese, Deborah Costakos, et al.
Journal of Genetic Counseling|February 6, 2007
Spiritual assessment in genetic counselingLinda M Reis, Robert Baumiller, William Scrivener, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|June 30, 2015
EFTUD2 deficiency in vertebrates: Identification of a novel human mutation and generation of a zebrafish modelBrett Deml, Linda M Reis, Sanaa Muheisen, et al.
Pageof 6