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

Sally Martell

Showing results (1-10 of 13) with videos related to

Pageof 2
Sort By:
BMC Medical Genetics|November 12, 2016
Exome sequencing identifies pathogenic variants of VPS13B in a patient with familial 16p11.2 duplicationJila Dastan, Chieko Chijiwa, Flamingo Tang, et al.
Journal of the American College of Cardiology|June 27, 2002
Nitroglycerin upregulates matrix metalloproteinase expression by human macrophagesAlison K Death, Shirley Nakhla, Kristine C Y McGrath, et al.
Molecular Human Reproduction|January 31, 2016
Whole exome sequencing in recurrent early pregnancy lossYing Qiao, Jiadi Wen, Flamingo Tang, et al.
Genes|March 25, 2022
Complex Autism Spectrum Disorder with Epilepsy, Strabismus and Self-Injurious Behaviors in a Patient with a De Novo Heterozygous <i>POLR2A</i> VariantDaniel R Evans, Ying Qiao, Brett Trost, et al.
Molecular Cytogenetics|February 13, 2015
Functional consequences of copy number variants in miscarriageJiadi Wen, Courtney W Hanna, Sally Martell, et al.
European Journal of Medical Genetics|June 17, 2018
Exome sequencing identified a de novo mutation of PURA gene in a patient with familial Xp22.31 microduplicationYing Qiao, Hani Bagheri, Flamingo Tang, et al.
Genes|August 6, 2021
Contribution of Multiple Inherited Variants to Autism Spectrum Disorder (ASD) in a Family with 3 Affected SiblingsJasleen Dhaliwal, Ying Qiao, Kristina Calli, et al.
American Journal of Medical Genetics. Part A|May 6, 2017
Whole exome sequencing of families with 1q21.1 microdeletion or microduplicationYing Qiao, Chansonette Badduke, Flamingo Tang, et al.
Genome|December 12, 2024
Uncovering the complexity of structural variants in four individuals with autism spectrum disorderSarah Dada, Katherine Dixon, Vahid Akbari, et al.
Orphanet Journal of Rare Diseases|July 11, 2013
Phenotypic and functional consequences of haploinsufficiency of genes from exocyst and retinoic acid pathway due to a recurrent microdeletion of 2p13.2Jiadi Wen, Fátima Lopes, Gabriela Soares, et al.
Pageof 2

Showing results (1-10 of 13) with videos related to

Sort By:
Pageof 2
BMC Medical Genetics|November 12, 2016
Exome sequencing identifies pathogenic variants of VPS13B in a patient with familial 16p11.2 duplicationJila Dastan, Chieko Chijiwa, Flamingo Tang, et al.
Journal of the American College of Cardiology|June 27, 2002
Nitroglycerin upregulates matrix metalloproteinase expression by human macrophagesAlison K Death, Shirley Nakhla, Kristine C Y McGrath, et al.
Molecular Human Reproduction|January 31, 2016
Whole exome sequencing in recurrent early pregnancy lossYing Qiao, Jiadi Wen, Flamingo Tang, et al.
Genes|March 25, 2022
Complex Autism Spectrum Disorder with Epilepsy, Strabismus and Self-Injurious Behaviors in a Patient with a De Novo Heterozygous <i>POLR2A</i> VariantDaniel R Evans, Ying Qiao, Brett Trost, et al.
Molecular Cytogenetics|February 13, 2015
Functional consequences of copy number variants in miscarriageJiadi Wen, Courtney W Hanna, Sally Martell, et al.
European Journal of Medical Genetics|June 17, 2018
Exome sequencing identified a de novo mutation of PURA gene in a patient with familial Xp22.31 microduplicationYing Qiao, Hani Bagheri, Flamingo Tang, et al.
Genes|August 6, 2021
Contribution of Multiple Inherited Variants to Autism Spectrum Disorder (ASD) in a Family with 3 Affected SiblingsJasleen Dhaliwal, Ying Qiao, Kristina Calli, et al.
American Journal of Medical Genetics. Part A|May 6, 2017
Whole exome sequencing of families with 1q21.1 microdeletion or microduplicationYing Qiao, Chansonette Badduke, Flamingo Tang, et al.
Genome|December 12, 2024
Uncovering the complexity of structural variants in four individuals with autism spectrum disorderSarah Dada, Katherine Dixon, Vahid Akbari, et al.
Orphanet Journal of Rare Diseases|July 11, 2013
Phenotypic and functional consequences of haploinsufficiency of genes from exocyst and retinoic acid pathway due to a recurrent microdeletion of 2p13.2Jiadi Wen, Fátima Lopes, Gabriela Soares, et al.
Pageof 2