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

David Chitayat

Showing results (171-180 of 353) with videos related to

Pageof 36
Sort By:
American Journal of Medical Genetics. Part A|August 18, 2016
Congenital limb deficiencies with vascular etiology: Possible association with maternal thrombophiliaLeslie Ordal, Johannes Keunen, Nicole Martin, et al.
American Journal of Medical Genetics. Part A|June 20, 2012
Middle and inner ear malformations in mutation-proven branchio-oculo-facial (BOF) syndrome: case series and review of the literatureMelissa T Carter, Susan Blaser, Blake Papsin, et al.
Journal of Autism and Developmental Disorders|July 12, 2012
Parents' perspectives on participating in genetic research in autismMagan Trottier, Wendy Roberts, Irene Drmic, et al.
Radiographics : a Review Publication of the Radiological Society of North America, Inc|January 20, 2004
Detection of fetal structural abnormalities with US during early pregnancyKatherine W Fong, Ants Toi, Shia Salem, et al.
Prenatal Diagnosis|June 6, 2024
Associations and outcomes of prenatally detected rhombencephalosynapsisYada Kunpalin, Elka Miller, Kamini Raghuram, et al.
Pediatric Blood & Cancer|September 13, 2018
"A change in perspective": Exploring the experiences of adolescents with hereditary tumor predispositionEvan Weber, Cheryl Shuman, Jonathan D Wasserman, et al.
Developmental Biology|June 14, 2008
Altered gene expression and methylation of the human chromosome 11 imprinted region in small for gestational age (SGA) placentaeLin Guo, Sanaa Choufani, Jose Ferreira, et al.
American Journal of Medical Genetics. Part A|September 12, 2012
Interstitial deletion of 11q-implicating the KIRREL3 gene in the neurocognitive delay associated with Jacobsen syndromeAndrea Guerin, Dimitri J Stavropoulos, Yaser Diab, et al.
Eye (London, England)|September 17, 2021
Gene therapy: perspectives from young adults with Leber's congenital amaurosisMelanie P Napier, Kavin Selvan, Robin Z Hayeems, et al.
Mitochondrion|October 6, 2010
Complex V TMEM70 deficiency results in mitochondrial nucleoid disorganizationJessie M Cameron, Valeriy Levandovskiy, Nevena Mackay, et al.
Pageof 36

Showing results (171-180 of 353) with videos related to

Sort By:
Pageof 36
American Journal of Medical Genetics. Part A|August 18, 2016
Congenital limb deficiencies with vascular etiology: Possible association with maternal thrombophiliaLeslie Ordal, Johannes Keunen, Nicole Martin, et al.
American Journal of Medical Genetics. Part A|June 20, 2012
Middle and inner ear malformations in mutation-proven branchio-oculo-facial (BOF) syndrome: case series and review of the literatureMelissa T Carter, Susan Blaser, Blake Papsin, et al.
Journal of Autism and Developmental Disorders|July 12, 2012
Parents' perspectives on participating in genetic research in autismMagan Trottier, Wendy Roberts, Irene Drmic, et al.
Radiographics : a Review Publication of the Radiological Society of North America, Inc|January 20, 2004
Detection of fetal structural abnormalities with US during early pregnancyKatherine W Fong, Ants Toi, Shia Salem, et al.
Prenatal Diagnosis|June 6, 2024
Associations and outcomes of prenatally detected rhombencephalosynapsisYada Kunpalin, Elka Miller, Kamini Raghuram, et al.
Pediatric Blood & Cancer|September 13, 2018
"A change in perspective": Exploring the experiences of adolescents with hereditary tumor predispositionEvan Weber, Cheryl Shuman, Jonathan D Wasserman, et al.
Developmental Biology|June 14, 2008
Altered gene expression and methylation of the human chromosome 11 imprinted region in small for gestational age (SGA) placentaeLin Guo, Sanaa Choufani, Jose Ferreira, et al.
American Journal of Medical Genetics. Part A|September 12, 2012
Interstitial deletion of 11q-implicating the KIRREL3 gene in the neurocognitive delay associated with Jacobsen syndromeAndrea Guerin, Dimitri J Stavropoulos, Yaser Diab, et al.
Eye (London, England)|September 17, 2021
Gene therapy: perspectives from young adults with Leber's congenital amaurosisMelanie P Napier, Kavin Selvan, Robin Z Hayeems, et al.
Mitochondrion|October 6, 2010
Complex V TMEM70 deficiency results in mitochondrial nucleoid disorganizationJessie M Cameron, Valeriy Levandovskiy, Nevena Mackay, et al.
Pageof 36