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

Thomas D Challman

Showing results (1-10 of 19) with videos related to

Pageof 2
Sort By:
American Journal of Medical Genetics. Part A|September 24, 2004
Congenital heart defects associated with Smith-Magenis syndrome: two cases of total anomalous pulmonary venous returnScott M Myers, Thomas D Challman
American Journal of Medical Genetics. Part A|July 3, 2007
End-stage renal failure in Smith-Magenis syndromeScott M Myers, Thomas D Challman, Glenn H Bock
Pediatric Clinics of North America|February 29, 2024
Etiologic Evaluation of Children with Autism Spectrum DisorderSteven M Lazar, Thomas D Challman, Scott M Myers
Journal of Autism and Developmental Disorders|May 22, 2003
The yield of the medical evaluation of children with pervasive developmental disordersThomas D Challman, William J Barbaresi, Slavica K Katusic, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 10, 2015
Shift happens: family background influences clinical variability in genetic neurodevelopmental disordersBrenda Finucane, Thomas D Challman, Christa Lese Martin, et al.
American Journal of Human Genetics|November 6, 2020
Response to Buxbaum et alScott M Myers, Thomas D Challman, Christa Leese Martin, et al.
Neurogenetics|March 15, 2017
Pain insensitivity: distal S6-segment mutations in Na<sub>V</sub>1.9 emerge as critical hotspotMargaret K King, Enrico Leipold, Jessica M Goehringer, et al.
Autism Research : Official Journal of the International Society for Autism Research|April 23, 2023
Letter to the editorBrenda Finucane, Scott M Myers, Thomas D Challman, et al.
The Lancet. Neurology|March 23, 2013
Developmental brain dysfunction: revival and expansion of old concepts based on new genetic evidenceAndres Moreno-De-Luca, Scott M Myers, Thomas D Challman, et al.
Human Mutation|October 13, 2018
The value of genomic variant ClinVar submissions from clinical providers: Beyond the addition of novel variantsKaren E Wain, Emily Palen, Juliann M Savatt, et al.
Pageof 2

Showing results (1-10 of 19) with videos related to

Sort By:
Pageof 2
American Journal of Medical Genetics. Part A|September 24, 2004
Congenital heart defects associated with Smith-Magenis syndrome: two cases of total anomalous pulmonary venous returnScott M Myers, Thomas D Challman
American Journal of Medical Genetics. Part A|July 3, 2007
End-stage renal failure in Smith-Magenis syndromeScott M Myers, Thomas D Challman, Glenn H Bock
Pediatric Clinics of North America|February 29, 2024
Etiologic Evaluation of Children with Autism Spectrum DisorderSteven M Lazar, Thomas D Challman, Scott M Myers
Journal of Autism and Developmental Disorders|May 22, 2003
The yield of the medical evaluation of children with pervasive developmental disordersThomas D Challman, William J Barbaresi, Slavica K Katusic, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 10, 2015
Shift happens: family background influences clinical variability in genetic neurodevelopmental disordersBrenda Finucane, Thomas D Challman, Christa Lese Martin, et al.
American Journal of Human Genetics|November 6, 2020
Response to Buxbaum et alScott M Myers, Thomas D Challman, Christa Leese Martin, et al.
Neurogenetics|March 15, 2017
Pain insensitivity: distal S6-segment mutations in Na<sub>V</sub>1.9 emerge as critical hotspotMargaret K King, Enrico Leipold, Jessica M Goehringer, et al.
Autism Research : Official Journal of the International Society for Autism Research|April 23, 2023
Letter to the editorBrenda Finucane, Scott M Myers, Thomas D Challman, et al.
The Lancet. Neurology|March 23, 2013
Developmental brain dysfunction: revival and expansion of old concepts based on new genetic evidenceAndres Moreno-De-Luca, Scott M Myers, Thomas D Challman, et al.
Human Mutation|October 13, 2018
The value of genomic variant ClinVar submissions from clinical providers: Beyond the addition of novel variantsKaren E Wain, Emily Palen, Juliann M Savatt, et al.
Pageof 2