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

Katja Doerschner

Showing results (41-50 of 45) with videos related to

Pageof 5
Sort By:
You have reached the last page of results.This site can display upto 45 results.
Diagnostic and Interventional Radiology (Ankara, Turkey)|November 9, 2018
Abnormal subcortical activity in congenital mirror movement disorder with RAD51 mutationPınar Demirayak, Onur Emre Onat, Aslıhan Örs Gevrekci, et al.
Neuroimage|April 8, 2018
Homozygous LAMC3 mutation links to structural and functional changes in visual attention networksBuse M Urgen, Yasemin Topac, F Seyhun Ustun, et al.
Brain and Behavior|June 14, 2021
Cortical connectivity in the face of congenital structural changes-A case of homozygous LAMC3 mutationPinar Demirayak, Kader Karli Oguz, Fatma Seyhun Ustun, et al.
Genome Research|September 3, 2011
Homozygosity mapping and targeted genomic sequencing reveal the gene responsible for cerebellar hypoplasia and quadrupedal locomotion in a consanguineous kindredSuleyman Gulsuner, Ayse Begum Tekinay, Katja Doerschner, et al.
Nature Genetics|May 17, 2011
Recessive LAMC3 mutations cause malformations of occipital cortical developmentTanyeri Barak, Kenneth Y Kwan, Angeliki Louvi, et al.
Pageof 5

Showing results (41-50 of 45) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 45 results.
Diagnostic and Interventional Radiology (Ankara, Turkey)|November 9, 2018
Abnormal subcortical activity in congenital mirror movement disorder with RAD51 mutationPınar Demirayak, Onur Emre Onat, Aslıhan Örs Gevrekci, et al.
Neuroimage|April 8, 2018
Homozygous LAMC3 mutation links to structural and functional changes in visual attention networksBuse M Urgen, Yasemin Topac, F Seyhun Ustun, et al.
Brain and Behavior|June 14, 2021
Cortical connectivity in the face of congenital structural changes-A case of homozygous LAMC3 mutationPinar Demirayak, Kader Karli Oguz, Fatma Seyhun Ustun, et al.
Genome Research|September 3, 2011
Homozygosity mapping and targeted genomic sequencing reveal the gene responsible for cerebellar hypoplasia and quadrupedal locomotion in a consanguineous kindredSuleyman Gulsuner, Ayse Begum Tekinay, Katja Doerschner, et al.
Nature Genetics|May 17, 2011
Recessive LAMC3 mutations cause malformations of occipital cortical developmentTanyeri Barak, Kenneth Y Kwan, Angeliki Louvi, et al.
Pageof 5