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

Christine M Armour

Showing results (1-10 of 60) with videos related to

Pageof 6
Sort By:
CMAJ : Canadian Medical Association Journal = Journal De L'Association Medicale Canadienne|April 9, 2014
Noninvasive prenatal testing from cell-free DNAChristine M Armour, Sarah M Nikkel
Journal of Genetic Counseling|November 6, 2015
Survey of the Definition of Fetal Viability and the Availability, Indications, and Decision Making Processes for Post-Viability Termination of Pregnancy for Fetal Abnormalities and Health Conditions in CanadaDanna Hull, Gregory Davies, Christine M Armour
Journal of Obstetrics and Gynaecology Canada : JOGC = Journal D'Obstetrique Et Gynecologie Du Canada : JOGC|June 30, 2012
Survey of prenatal counselling practices regarding aneuploidy risk modification, invasive diagnostic procedure risks, and procedure eligibility criteria in Canadian centresDanna Hull, Gregory Davies, Christine M Armour
American Journal of Medical Genetics. Part A|August 21, 2012
Microdeletion on 3p25 in a patient with features of 3p deletion syndromeIskra T Peltekova, Athen Macdonald, Christine M Armour
American Journal of Medical Genetics. Part A|September 27, 2014
Novel interstitial deletion of 10q24.3-25.1 associated with multiple congenital anomalies including lobar holoprosencephaly, cleft lip and palate, and hypoplastic kidneysIskra T Peltekova, Julie Hurteau-Millar, Christine M Armour
Plos One|October 2, 2015
Further Insights into the Allan-Herndon-Dudley Syndrome: Clinical and Functional Characterization of a Novel MCT8 MutationChristine M Armour, Simone Kersseboom, Grace Yoon, et al.
CMAJ Open|October 7, 2018
Trends in the use of prenatal testing services for fetal aneuploidy in Ontario: a descriptive studyTianhua Huang, Shelley Dougan, Mark Walker, et al.
American Journal of Medical Genetics. Part A|September 18, 2009
Fitzsimmons syndrome: spastic paraplegia, brachydactyly and cognitive impairmentChristine M Armour, Peter Humphreys, Raoul C M Hennekam, et al.
Pediatric Dermatology|September 23, 2020
Cutaneous granulomas as the presenting manifestation of Griscelli syndrome type 2Ryan Gotesman, Michele Ramien, Christine M Armour, et al.
American Journal of Medical Genetics. Part A|February 19, 2019
NID1 variant associated with occipital cephaloceles in a family expressing a spectrum of phenotypesVanda McNiven, Yoko A Ito, Taila Hartley, et al.
Pageof 6

Showing results (1-10 of 60) with videos related to

Sort By:
Pageof 6
CMAJ : Canadian Medical Association Journal = Journal De L'Association Medicale Canadienne|April 9, 2014
Noninvasive prenatal testing from cell-free DNAChristine M Armour, Sarah M Nikkel
Journal of Genetic Counseling|November 6, 2015
Survey of the Definition of Fetal Viability and the Availability, Indications, and Decision Making Processes for Post-Viability Termination of Pregnancy for Fetal Abnormalities and Health Conditions in CanadaDanna Hull, Gregory Davies, Christine M Armour
Journal of Obstetrics and Gynaecology Canada : JOGC = Journal D'Obstetrique Et Gynecologie Du Canada : JOGC|June 30, 2012
Survey of prenatal counselling practices regarding aneuploidy risk modification, invasive diagnostic procedure risks, and procedure eligibility criteria in Canadian centresDanna Hull, Gregory Davies, Christine M Armour
American Journal of Medical Genetics. Part A|August 21, 2012
Microdeletion on 3p25 in a patient with features of 3p deletion syndromeIskra T Peltekova, Athen Macdonald, Christine M Armour
American Journal of Medical Genetics. Part A|September 27, 2014
Novel interstitial deletion of 10q24.3-25.1 associated with multiple congenital anomalies including lobar holoprosencephaly, cleft lip and palate, and hypoplastic kidneysIskra T Peltekova, Julie Hurteau-Millar, Christine M Armour
Plos One|October 2, 2015
Further Insights into the Allan-Herndon-Dudley Syndrome: Clinical and Functional Characterization of a Novel MCT8 MutationChristine M Armour, Simone Kersseboom, Grace Yoon, et al.
CMAJ Open|October 7, 2018
Trends in the use of prenatal testing services for fetal aneuploidy in Ontario: a descriptive studyTianhua Huang, Shelley Dougan, Mark Walker, et al.
American Journal of Medical Genetics. Part A|September 18, 2009
Fitzsimmons syndrome: spastic paraplegia, brachydactyly and cognitive impairmentChristine M Armour, Peter Humphreys, Raoul C M Hennekam, et al.
Pediatric Dermatology|September 23, 2020
Cutaneous granulomas as the presenting manifestation of Griscelli syndrome type 2Ryan Gotesman, Michele Ramien, Christine M Armour, et al.
American Journal of Medical Genetics. Part A|February 19, 2019
NID1 variant associated with occipital cephaloceles in a family expressing a spectrum of phenotypesVanda McNiven, Yoko A Ito, Taila Hartley, et al.
Pageof 6