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

I Filges

Showing results (1-10 of 6) with videos related to

Pageof 1
Sort By:
Ultraschall in Der Medizin (Stuttgart, Germany : 1980)|October 16, 2015
An Appeal for Ultrasound and Current GuidelinesS Tercanli, I Filges
Journal of Bioethical Inquiry|July 22, 2024
Attitudes Towards Non-directiveness Among Medical Geneticists in Germany and SwitzerlandJ Eichinger, B S Elger, S McLennan, et al.
Molecular Human Reproduction|December 16, 2014
Recurrent triploidy due to a failure to complete maternal meiosis II: whole-exome sequencing reveals candidate variantsI Filges, I Manokhina, M S Peñaherrera, et al.
Clinical Genetics|November 25, 2010
Deletion in Xp22.11: PTCHD1 is a candidate gene for X-linked intellectual disability with or without autismI Filges, B Röthlisberger, A Blattner, et al.
Clinical Genetics|October 17, 2013
Exome sequencing identifies mutations in KIF14 as a novel cause of an autosomal recessive lethal fetal ciliopathy phenotypeI Filges, E Nosova, E Bruder, et al.
Clinical Genetics|August 19, 2014
Phenotypic spectrum associated with PTCHD1 deletions and truncating mutations includes intellectual disability and autism spectrum disorderA Chaudhry, A Noor, B Degagne, et al.
Pageof 1

Showing results (1-10 of 6) with videos related to

Sort By:
Pageof 1
Ultraschall in Der Medizin (Stuttgart, Germany : 1980)|October 16, 2015
An Appeal for Ultrasound and Current GuidelinesS Tercanli, I Filges
Journal of Bioethical Inquiry|July 22, 2024
Attitudes Towards Non-directiveness Among Medical Geneticists in Germany and SwitzerlandJ Eichinger, B S Elger, S McLennan, et al.
Molecular Human Reproduction|December 16, 2014
Recurrent triploidy due to a failure to complete maternal meiosis II: whole-exome sequencing reveals candidate variantsI Filges, I Manokhina, M S Peñaherrera, et al.
Clinical Genetics|November 25, 2010
Deletion in Xp22.11: PTCHD1 is a candidate gene for X-linked intellectual disability with or without autismI Filges, B Röthlisberger, A Blattner, et al.
Clinical Genetics|October 17, 2013
Exome sequencing identifies mutations in KIF14 as a novel cause of an autosomal recessive lethal fetal ciliopathy phenotypeI Filges, E Nosova, E Bruder, et al.
Clinical Genetics|August 19, 2014
Phenotypic spectrum associated with PTCHD1 deletions and truncating mutations includes intellectual disability and autism spectrum disorderA Chaudhry, A Noor, B Degagne, et al.
Pageof 1