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Trends in Neurosciences|January 13, 2009
Contact in the genetics of autism and schizophreniaJ Peter H Burbach, Bert van der ZwaagAdvances in Protein Chemistry and Structural Biology|August 18, 2011
Contactins: structural aspects in relation to developmental functions in brain diseaseAmila Zuko, Samuel Bouyain, Bert van der Zwaag, et al.Neurology|August 13, 2003
Möbius syndrome redefined: a syndrome of rhombencephalic maldevelopmentHarriëtte T F M Verzijl, Bert van der Zwaag, Johannes R M Cruysberg, et al.Brain Research. Developmental Brain Research|July 6, 2005
Nucleotide variation analysis does not support a causal role for plexin-A1 in hereditary congenital facial paresisBert van der Zwaag, J Peter H Burbach, Han G Brunner, et al.Cell Adhesion & Migration|March 5, 2016
Developmental role of the cell adhesion molecule Contactin-6 in the cerebral cortex and hippocampusAmila Zuko, Asami Oguro-Ando, Roland van Dijk, et al.Molecular Genetics & Genomic Medicine|May 6, 2019
Genetic analysis in the bariatric clinic; impact of a PTEN gene mutationMellody I Cooiman, Lotte Kleinendorst, Bert van der Zwaag, et al.European Journal of Pediatrics|February 12, 2017
A novel mutation of laminin β2 (LAMB2) in two siblings with renal failureFarah A Falix, Carlien A M Bennebroek, Bert van der Zwaag, et al.Genomics|June 15, 2005
Identifying new candidate genes for hereditary facial paresis on chromosome 3q21-q22 by RNA in situ hybridization in mouseBert van der Zwaag, J Peter H Burbach, Curt Scharfe, et al.Kidney International Reports|September 18, 2024
The Importance of Copy Number Variant Analysis in Patients with Monogenic Kidney DiseaseLaura R Claus, Robert F Ernst, Martin G Elferink, et al.Hemasphere|November 15, 2019
The Complexity of Genotype-Phenotype Correlations in Hereditary Spherocytosis: A Cohort of 95 Patients: Genotype-Phenotype Correlation in Hereditary SpherocytosisAnnelies van Vuren, Bert van der Zwaag, Rick Huisjes, et al.Pageof 7