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

Daryl A Scott

Showing results (71-80 of 128) with videos related to

Pageof 13
Sort By:
American Journal of Medical Genetics. Part A|July 4, 2007
Microarray-based CGH detects chromosomal mosaicism not revealed by conventional cytogeneticsSau W Cheung, Chad A Shaw, Daryl A Scott, et al.
Ophthalmic Epidemiology|December 21, 2020
A Comprehensive Assessment of Co-occurring Birth Defects among Infants with Non-Syndromic Anophthalmia or MicrophthalmiaJeremy M Schraw, Renata H Benjamin, Daryl A Scott, et al.
American Journal of Medical Genetics. Part A|March 22, 2021
Patterns of congenital anomalies among individuals with trisomy 13 in TexasDiego Diaz, Renata H Benjamin, Maria Luisa Navarro Sanchez, et al.
Journal of Medical Genetics|April 29, 2011
Genomic alterations that contribute to the development of isolated and non-isolated congenital diaphragmatic herniaMargaret J Wat, Danielle Veenma, Jacob Hogue, et al.
American Journal of Medical Genetics. Part A|September 5, 2020
Birth defects that co-occur with non-syndromic gastroschisis and omphaloceleOmobola O Oluwafemi, Renata H Benjamin, Maria Luisa Navarro Sanchez, et al.
Journal of Medical Genetics|June 11, 2020
<i>NUBPL</i> mitochondrial disease: new patients and review of the genetic and clinical spectrumVirginia Kimonis, Rehab Al Dubaisi, Andrew E Maclean, et al.
EMBO Reports|August 8, 2023
Sox7-positive endothelial progenitors establish coronary arteries and govern ventricular compactionIvy Kn Chiang, David Humphrey, Richard J Mills, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 1, 2023
Monoallelic loss-of-function BMP2 variants result in BMP2-related skeletal dysplasia spectrumJessica R C Priestley, Ashish R Deshwar, Harsha Murthy, et al.
Human Mutation|January 31, 2020
BAZ2B haploinsufficiency as a cause of developmental delay, intellectual disability, and autism spectrum disorderTiana M Scott, Hui Guo, Evan E Eichler, et al.
JCI Insight|May 8, 2024
Exome sequencing implicates ancestry-related Mendelian variation at SYNE1 in childhood-onset essential hypertensionIan Copeland, Edmond Wonkam-Tingang, Monesha Gupta-Malhotra, et al.
Pageof 13

Showing results (71-80 of 128) with videos related to

Sort By:
Pageof 13
American Journal of Medical Genetics. Part A|July 4, 2007
Microarray-based CGH detects chromosomal mosaicism not revealed by conventional cytogeneticsSau W Cheung, Chad A Shaw, Daryl A Scott, et al.
Ophthalmic Epidemiology|December 21, 2020
A Comprehensive Assessment of Co-occurring Birth Defects among Infants with Non-Syndromic Anophthalmia or MicrophthalmiaJeremy M Schraw, Renata H Benjamin, Daryl A Scott, et al.
American Journal of Medical Genetics. Part A|March 22, 2021
Patterns of congenital anomalies among individuals with trisomy 13 in TexasDiego Diaz, Renata H Benjamin, Maria Luisa Navarro Sanchez, et al.
Journal of Medical Genetics|April 29, 2011
Genomic alterations that contribute to the development of isolated and non-isolated congenital diaphragmatic herniaMargaret J Wat, Danielle Veenma, Jacob Hogue, et al.
American Journal of Medical Genetics. Part A|September 5, 2020
Birth defects that co-occur with non-syndromic gastroschisis and omphaloceleOmobola O Oluwafemi, Renata H Benjamin, Maria Luisa Navarro Sanchez, et al.
Journal of Medical Genetics|June 11, 2020
<i>NUBPL</i> mitochondrial disease: new patients and review of the genetic and clinical spectrumVirginia Kimonis, Rehab Al Dubaisi, Andrew E Maclean, et al.
EMBO Reports|August 8, 2023
Sox7-positive endothelial progenitors establish coronary arteries and govern ventricular compactionIvy Kn Chiang, David Humphrey, Richard J Mills, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 1, 2023
Monoallelic loss-of-function BMP2 variants result in BMP2-related skeletal dysplasia spectrumJessica R C Priestley, Ashish R Deshwar, Harsha Murthy, et al.
Human Mutation|January 31, 2020
BAZ2B haploinsufficiency as a cause of developmental delay, intellectual disability, and autism spectrum disorderTiana M Scott, Hui Guo, Evan E Eichler, et al.
JCI Insight|May 8, 2024
Exome sequencing implicates ancestry-related Mendelian variation at SYNE1 in childhood-onset essential hypertensionIan Copeland, Edmond Wonkam-Tingang, Monesha Gupta-Malhotra, et al.
Pageof 13