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

Arthur L Beaudet

Showing results (111-120 of 190) with videos related to

Pageof 19
Sort By:
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 19, 2005
Development and validation of a CGH microarray for clinical cytogenetic diagnosisSau W Cheung, Chad A Shaw, Wei Yu, et al.
Prenatal Diagnosis|February 27, 2024
Noninvasive single-cell-based prenatal genetic testing: A proof of concept clinical studyMichelle Bellair, Elisabete Amaral, Mason Ouren, et al.
American Journal of Medical Genetics. Part A|September 25, 2004
A mixed epigenetic/genetic model for oligogenic inheritance of autism with a limited role for UBE3AYong-Hui Jiang, Trilochan Sahoo, Ron C Michaelis, et al.
Journal of Inherited Metabolic Disease|May 27, 2016
Erratum to: Untargeted metabolomic analysis for the clinical screening of inborn errors of metabolismMarcus J Miller, Adam D Kennedy, Andrea D Eckhart, et al.
Elife|January 3, 2023
Antisense oligonucleotide therapy rescues disturbed brain rhythms and sleep in juvenile and adult mouse models of Angelman syndromeDongwon Lee, Wu Chen, Heet Naresh Kaku, et al.
Elife|October 15, 2024
Correction: Antisense oligonucleotide therapy rescues disturbed brain rhythms and sleep in juvenile and adult mouse models of Angelman syndromeDongwon Lee, Wu Chen, Heet Naresh Kaku, et al.
BMC Biology|June 22, 2018
Comparative analysis of single-stranded DNA donors to generate conditional null mouse allelesDenise G Lanza, Angelina Gaspero, Isabel Lorenzo, et al.
Journal of Inherited Metabolic Disease|April 16, 2015
Untargeted metabolomic analysis for the clinical screening of inborn errors of metabolismMarcus J Miller, Adam D Kennedy, Andrea D Eckhart, et al.
Prenatal Diagnosis|October 21, 2016
Genome-wide copy number analysis on DNA from fetal cells isolated from the blood of pregnant womenSteen Kølvraa, Ripudaman Singh, Elizabeth A Normand, et al.
Nature Genetics|November 10, 2009
A small recurrent deletion within 15q13.3 is associated with a range of neurodevelopmental phenotypesMarwan Shinawi, Christian P Schaaf, Samarth S Bhatt, et al.
Pageof 19

Showing results (111-120 of 190) with videos related to

Sort By:
Pageof 19
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 19, 2005
Development and validation of a CGH microarray for clinical cytogenetic diagnosisSau W Cheung, Chad A Shaw, Wei Yu, et al.
Prenatal Diagnosis|February 27, 2024
Noninvasive single-cell-based prenatal genetic testing: A proof of concept clinical studyMichelle Bellair, Elisabete Amaral, Mason Ouren, et al.
American Journal of Medical Genetics. Part A|September 25, 2004
A mixed epigenetic/genetic model for oligogenic inheritance of autism with a limited role for UBE3AYong-Hui Jiang, Trilochan Sahoo, Ron C Michaelis, et al.
Journal of Inherited Metabolic Disease|May 27, 2016
Erratum to: Untargeted metabolomic analysis for the clinical screening of inborn errors of metabolismMarcus J Miller, Adam D Kennedy, Andrea D Eckhart, et al.
Elife|January 3, 2023
Antisense oligonucleotide therapy rescues disturbed brain rhythms and sleep in juvenile and adult mouse models of Angelman syndromeDongwon Lee, Wu Chen, Heet Naresh Kaku, et al.
Elife|October 15, 2024
Correction: Antisense oligonucleotide therapy rescues disturbed brain rhythms and sleep in juvenile and adult mouse models of Angelman syndromeDongwon Lee, Wu Chen, Heet Naresh Kaku, et al.
BMC Biology|June 22, 2018
Comparative analysis of single-stranded DNA donors to generate conditional null mouse allelesDenise G Lanza, Angelina Gaspero, Isabel Lorenzo, et al.
Journal of Inherited Metabolic Disease|April 16, 2015
Untargeted metabolomic analysis for the clinical screening of inborn errors of metabolismMarcus J Miller, Adam D Kennedy, Andrea D Eckhart, et al.
Prenatal Diagnosis|October 21, 2016
Genome-wide copy number analysis on DNA from fetal cells isolated from the blood of pregnant womenSteen Kølvraa, Ripudaman Singh, Elizabeth A Normand, et al.
Nature Genetics|November 10, 2009
A small recurrent deletion within 15q13.3 is associated with a range of neurodevelopmental phenotypesMarwan Shinawi, Christian P Schaaf, Samarth S Bhatt, et al.
Pageof 19