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 (151-160 of 353) with videos related to

Pageof 36
Sort By:
Prenatal Diagnosis|April 25, 2019
Impact of introduction of noninvasive prenatal testing on uptake of genetic testing in fetuses with central nervous system anomaliesSamar Al Toukhi, David Chitayat, Johannes Keunen, et al.
Pediatric Radiology|June 14, 2006
Prenatal detection of microtia by MRI in a fetus with trisomy 22Andrea Milic, Susan Blaser, Ashley Robinson, et al.
F&S Reports|January 11, 2024
Challenges experienced by genetic counselors while they provided counseling about mosaic embryosOlivia M Moran, Kayla Flamenbaum, Diane Myles Reid, et al.
Prenatal Diagnosis|February 27, 2009
Cornelia de Lange syndrome (CdLS): prenatal and autopsy findingsKaren Chong, Sarah Keating, Stephanie Hurst, et al.
Prenatal Diagnosis|July 22, 2005
Cavum veli interpositi: prenatal diagnosis and postnatal outcomePrakesh S Shah, Susan Blaser, Ants Toi, et al.
Prenatal Diagnosis|November 7, 2006
X-Linked dominant chondrodysplasia punctata: prenatal diagnosis and autopsy findingsShalini Umranikar, Phyllis Glanc, Sheila Unger, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|September 28, 2006
A novel GDAP1 mutation 439delA is associated with autosomal recessive CMT diseaseDomna-Maria Georgiou, Paschalis Nicolaou, David Chitayat, et al.
American Journal of Human Genetics|May 23, 2002
Connection between elastin haploinsufficiency and increased cell proliferation in patients with supravalvular aortic stenosis and Williams-Beuren syndromeZsolt Urbán, Sheila Riazi, Thomas L Seidl, et al.
Prenatal Diagnosis|December 10, 2016
Mutations in the NEB gene cause fetal akinesia/arthrogryposis multiplex congenitaMichal Feingold-Zadok, David Chitayat, Karen Chong, et al.
Ultraschall in Der Medizin (Stuttgart, Germany : 1980)|June 24, 2020
Fetal Meconium Peritonitis - Prenatal Findings and Postnatal Outcome: A Case Series, Systematic Review, and Meta-AnalysisShiri Shinar, Swati Agrawal, Michelle Ryu, et al.
Pageof 36

Showing results (151-160 of 353) with videos related to

Sort By:
Pageof 36
Prenatal Diagnosis|April 25, 2019
Impact of introduction of noninvasive prenatal testing on uptake of genetic testing in fetuses with central nervous system anomaliesSamar Al Toukhi, David Chitayat, Johannes Keunen, et al.
Pediatric Radiology|June 14, 2006
Prenatal detection of microtia by MRI in a fetus with trisomy 22Andrea Milic, Susan Blaser, Ashley Robinson, et al.
F&S Reports|January 11, 2024
Challenges experienced by genetic counselors while they provided counseling about mosaic embryosOlivia M Moran, Kayla Flamenbaum, Diane Myles Reid, et al.
Prenatal Diagnosis|February 27, 2009
Cornelia de Lange syndrome (CdLS): prenatal and autopsy findingsKaren Chong, Sarah Keating, Stephanie Hurst, et al.
Prenatal Diagnosis|July 22, 2005
Cavum veli interpositi: prenatal diagnosis and postnatal outcomePrakesh S Shah, Susan Blaser, Ants Toi, et al.
Prenatal Diagnosis|November 7, 2006
X-Linked dominant chondrodysplasia punctata: prenatal diagnosis and autopsy findingsShalini Umranikar, Phyllis Glanc, Sheila Unger, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|September 28, 2006
A novel GDAP1 mutation 439delA is associated with autosomal recessive CMT diseaseDomna-Maria Georgiou, Paschalis Nicolaou, David Chitayat, et al.
American Journal of Human Genetics|May 23, 2002
Connection between elastin haploinsufficiency and increased cell proliferation in patients with supravalvular aortic stenosis and Williams-Beuren syndromeZsolt Urbán, Sheila Riazi, Thomas L Seidl, et al.
Prenatal Diagnosis|December 10, 2016
Mutations in the NEB gene cause fetal akinesia/arthrogryposis multiplex congenitaMichal Feingold-Zadok, David Chitayat, Karen Chong, et al.
Ultraschall in Der Medizin (Stuttgart, Germany : 1980)|June 24, 2020
Fetal Meconium Peritonitis - Prenatal Findings and Postnatal Outcome: A Case Series, Systematic Review, and Meta-AnalysisShiri Shinar, Swati Agrawal, Michelle Ryu, et al.
Pageof 36