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Deepti Anand

Showing results (31-40 of 42) with videos related to

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Journal of Medical Genetics|May 27, 2019
Pathogenic variants in <i>PLOD3</i> result in a Stickler syndrome-like connective tissue disorder with vascular complicationsLisa Jean Ewans, Alison Colley, Carles Gaston-Massuet, et al.
Human Genetics|November 24, 2016
Novel phenotypes and loci identified through clinical genomics approaches to pediatric cataractNisha Patel, Deepti Anand, Dorota Monies, et al.
Research Square|March 11, 2024
Rare Variants Analyses Suggest Novel Cleft Genes in the African PopulationAzeez Alade, Peter Mossey, Waheed Awotoye, et al.
Scientific Reports|June 20, 2024
Rare variants analyses suggest novel cleft genes in the African populationAzeez Alade, Peter Mossey, Waheed Awotoye, et al.
Genetic Epidemiology|April 18, 2024
Shared genetic risk between major orofacial cleft phenotypes in an African populationAzeez Alade, Tabitha Peter, Tamara Busch, et al.
Genetic Epidemiology|June 8, 2019
A systematic genetic analysis and visualization of phenotypic heterogeneity among orofacial cleft GWAS signalsJenna C Carlson, Deepti Anand, Azeez Butali, et al.
Frontiers in Genetics|October 17, 2019
<i>Missense Pathogenic variants in KIF4A</i> Affect Dental Morphogenesis Resulting in X-linked Taurodontism, Microdontia and Dens-InvaginatusLord J J Gowans, Sophia Cameron-Christie, Rebecca L Slayton, et al.
Human Mutation|June 20, 2019
Mutations in GDF11 and the extracellular antagonist, Follistatin, as a likely cause of Mendelian forms of orofacial clefting in humansTimothy C Cox, Andrew C Lidral, Jason C McCoy, et al.
American Journal of Human Genetics|May 29, 2018
Mutations in the Epithelial Cadherin-p120-Catenin Complex Cause Mendelian Non-Syndromic Cleft Lip with or without Cleft PalateLiza L Cox, Timothy C Cox, Lina M Moreno Uribe, et al.
Scientific Reports|July 11, 2022
Whole-genome sequencing reveals de-novo mutations associated with nonsyndromic cleft lip/palateWaheed Awotoye, Peter A Mossey, Jacqueline B Hetmanski, et al.
Pageof 5

Showing results (31-40 of 42) with videos related to

Sort By:
Pageof 5
Journal of Medical Genetics|May 27, 2019
Pathogenic variants in <i>PLOD3</i> result in a Stickler syndrome-like connective tissue disorder with vascular complicationsLisa Jean Ewans, Alison Colley, Carles Gaston-Massuet, et al.
Human Genetics|November 24, 2016
Novel phenotypes and loci identified through clinical genomics approaches to pediatric cataractNisha Patel, Deepti Anand, Dorota Monies, et al.
Research Square|March 11, 2024
Rare Variants Analyses Suggest Novel Cleft Genes in the African PopulationAzeez Alade, Peter Mossey, Waheed Awotoye, et al.
Scientific Reports|June 20, 2024
Rare variants analyses suggest novel cleft genes in the African populationAzeez Alade, Peter Mossey, Waheed Awotoye, et al.
Genetic Epidemiology|April 18, 2024
Shared genetic risk between major orofacial cleft phenotypes in an African populationAzeez Alade, Tabitha Peter, Tamara Busch, et al.
Genetic Epidemiology|June 8, 2019
A systematic genetic analysis and visualization of phenotypic heterogeneity among orofacial cleft GWAS signalsJenna C Carlson, Deepti Anand, Azeez Butali, et al.
Frontiers in Genetics|October 17, 2019
<i>Missense Pathogenic variants in KIF4A</i> Affect Dental Morphogenesis Resulting in X-linked Taurodontism, Microdontia and Dens-InvaginatusLord J J Gowans, Sophia Cameron-Christie, Rebecca L Slayton, et al.
Human Mutation|June 20, 2019
Mutations in GDF11 and the extracellular antagonist, Follistatin, as a likely cause of Mendelian forms of orofacial clefting in humansTimothy C Cox, Andrew C Lidral, Jason C McCoy, et al.
American Journal of Human Genetics|May 29, 2018
Mutations in the Epithelial Cadherin-p120-Catenin Complex Cause Mendelian Non-Syndromic Cleft Lip with or without Cleft PalateLiza L Cox, Timothy C Cox, Lina M Moreno Uribe, et al.
Scientific Reports|July 11, 2022
Whole-genome sequencing reveals de-novo mutations associated with nonsyndromic cleft lip/palateWaheed Awotoye, Peter A Mossey, Jacqueline B Hetmanski, et al.
Pageof 5