Showing results (311-320 of 323) with videos related to

Sort By:
Pageof 33
Prenatal Diagnosis|July 8, 2025
Open Spinal Dysraphism Without Hindbrain Herniation-Natural History and Postnatal OutcomeI Bedei, C C Kik, R Axt-Fliedner, et al.
American Journal of Human Genetics|May 11, 2006
Mutations in the gene encoding peroxisomal sterol carrier protein X (SCPx) cause leukencephalopathy with dystonia and motor neuropathyS Ferdinandusse, P Kostopoulos, S Denis, et al.
Molecular and Cellular Biology|May 4, 2004
The transcription factor RFX3 directs nodal cilium development and left-right asymmetry specificationE Bonnafe, M Touka, A AitLounis, et al.
Human Molecular Genetics|May 23, 1998
Genetic and molecular definition of complementation group D in MHC class II deficiencyM C Fondaneche, J Villard, W Wiszniewski, et al.
Laboratory Investigation; a Journal of Technical Methods and Pathology|August 11, 2010
Gene delivery of TGF-β1 induces arthrofibrosis and chondrometaplasia of synovium in vivoRachael S Watson, Elvire Gouze, Padraic P Levings, et al.
European Archives of Psychiatry and Clinical Neuroscience|June 25, 2014
Influence of DGKH variants on amygdala volume in patients with bipolar affective disorder and schizophreniaS Kittel-Schneider, T Wobrock, H Scherk, et al.
AJNR. American Journal of Neuroradiology|March 3, 2020
The FRED for Cerebral Aneurysms of the Posterior Circulation: A Subgroup Analysis of the EuFRED RegistryC J Griessenauer, M A Möhlenbruch, P Hendrix, et al.
Pageof 33