Williams-Beuren SyndromeAguilar, Patricia VZeng, H U ISolorzano, AliciaSwayne, David ECox, Nancy JKatz, Jacqueline MTaubenberger, Jeffery KPalese, Peter
Williams-Beuren syndrome (WBS; also called Williams syndrome) is a multisystem developmental disorder that is almost always associated with an approx 1.5-Mb deletion of chromosome 7q11.23 (OMIM no. 194050). The deletion was identified in 1993 based on the observation of phenotypic overlap with sup...
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4Wellcome Trust Sanger Institute, Cambridge, UK; 5Center for Integrative Genomics, University of Lausanne, Lausanne, Switzerland Williams –Beuren syndrome (WBS) is a neurodevelopmental and multisystemic disease that results from hemizygosity of approximately 25 genes mapping to chromosomal region 7q11.23...
Williams-Beuren Syndrome Chromosome Region 16 Antibody is a Rabbit Polyclonal antibody against Williams-Beuren Syndrome Chromosome Region 16.
Williams-Beuren syndrome, or Williams syndrome, is caused by a contiguous gene deletion at 7q11.23 that encompasses the elastin geneELN.66,67Similar to 22q11.2 deletion syndrome, deletions are often sporadic but can be inherited. Between 50% and 80% of patients with Williams syndrome have CHD...
'Williams Syndrome (Williams-Beuren syndrome, WMS)' published in 'Encyclopedia of Genetics, Genomics, Proteomics and Informatics'
Williams-Beuren syndrome is a complex developmental disorder characterised by congenital heart and vascular disease, mental retardation, a characteristic learning profile, a hypersocial personality and infantile hypercalcaemia. Severe aortic obstruction in Williams-Beuren syndrome--a short case series Williams...
Williams–Beuren syndrome (WBS) is a multisystemic genetic disorder caused by a contiguous gene deletion at 7q11.23. We report a severely affected WBS patient with cerebral and cerebellar dysplasia as well as hypertrophic cardiomyopathy. Microarray comparative genomic hybridization (aCGH) detected a del...