Hemizygosity of δ-Catenin (CTNND2) Is Associated with Severe Mental Retardation in Cri-du-Chat Syndrome
- 1 January 2000
- Vol. 63 (2) , 157-164
- https://doi.org/10.1006/geno.1999.6090
Abstract
No abstract availableKeywords
This publication has 27 references indexed in Scilit:
- Mice Lacking p35, a Neuronal Specific Activator of Cdk5, Display Cortical Lamination Defects, Seizures, and Adult LethalityPublished by Elsevier ,2014
- Mutations in filamin 1 Prevent Migration of Cerebral Cortical Neurons in Human Periventricular HeterotopiaNeuron, 1998
- A Novel CNS Gene Required for Neuronal Migration and Involved in X-Linked Subcortical Laminar Heterotopia and Lissencephaly SyndromeCell, 1998
- doublecortin, a Brain-Specific Gene Mutated in Human X-Linked Lissencephaly and Double Cortex Syndrome, Encodes a Putative Signaling ProteinCell, 1998
- Mechanism and regulation of mRNA polyadenylationGenes & Development, 1997
- Gapped BLAST and PSI-BLAST: a new generation of protein database search programsNucleic Acids Research, 1997
- A High-Resolution Physical and Transcript Map of the Cri du Chat Region of Human Chromosome 5pGenome Research, 1997
- A protein related to extracellular matrix proteins deleted in the mouse mutant reelerNature, 1995
- Physical Mapping of Genetic Markers on the Short Arm of Chromosome 5Genomics, 1994
- A Yeast Artificial Chromosome Contig of the Critical Region for Cri-du-Chat SyndromeGenomics, 1994