Williams syndrome (WS), also Williams–Beuren syndrome (WBS), is a genetic disorder that affects many parts of the body. Facial features frequently include...

duplication syndrome (also called dup7 or 7dup or duplication of the Williams-Beuren syndrome critical region) is a rare genetic syndrome caused by micro-duplication...

to be a higher prevalence of left-eye dominance in those with Williams–Beuren syndrome, and possibly in migraine sufferers as well. Eye dominance has...

lack of fear in dogs may include genetic modifications related to Williams-Beuren syndrome in humans, which cause hypersociability at the expense of problem-solving...

Reymond A (August 2006). "Submicroscopic deletion in patients with Williams-Beuren syndrome influences expression levels of the nonhemizygous flanking genes"...

in the treatment of arterial wall hypertrophy in children with Williams Beuren Syndrome: a randomized controlled trial". BMC Pediatrics. 19 (1): 170. doi:10...

individuals with Ehlers-Danlos syndrome, Marfan syndrome, Loeys–Dietz syndrome, Williams–Beuren syndrome or polycystic kidney disease. Other risk factors...

et al. (August 2006). "Submicroscopic deletion in patients with Williams-Beuren syndrome influences expression levels of the nonhemizygous flanking genes"...

Warsaw, Poland Beckwith-Wiedemann syndrome, or Wiedemann Beckwith Syndrome, a genetic disorder Williams-Beuren syndrome, a rare genetic disorder WBS Penguins...

DnaJ homolog subfamily C member 30 (DNAJC30), also known as Williams Beuren syndrome chromosome region 18 protein (WBSCR18), is a protein that in humans...

I; et al. (2006). "Echocardiographic findings in patients with Williams-Beuren syndrome". Wiener Klinische Wochenschrift. 118 (17–18): 538–42. doi:10...

ChREBP promotes glycolysis and lipogenesis. This gene is deleted in Williams-Beuren syndrome, a multisystem developmental disorder caused by the deletion of...

Clarkson, Patricia M.; Berdon, Walter E. (2010). "John C. P. Williams of Williams-Beuren syndrome". Pediatric Radiology. 41 (2): 267–269. doi:10.1007/s00247-010-1909-y...

variation in the GTF2I and GTF2IRD1 genes at the locus responsible for Williams-Beuren Syndrome in humans is also associated with hypersociability in dogs. Genes...

variation in the genes that are associated with human Williams-Beuren syndrome. This syndrome causes increased hyper-sociability, which may have been...

A (Jun 2002). "Identification of additional transcripts in the Williams-Beuren syndrome critical region". Hum Genet. 110 (5): 429–38. doi:10.1007/s00439-002-0710-x...

Williams-Beuren syndrome". Cytogenet Cell Genet. 95 (1–2): 20–7. doi:10.1159/000057012. PMID 11978965. S2CID 21992204. "Entrez Gene: WBSCR22 Williams...

Clarkson, Patricia M.; Berdon, Walter E. (2010). "John C. P. Williams of Williams-Beuren syndrome". Pediatric Radiology. 41 (2): 267–269. doi:10.1007/s00247-010-1909-y...

System at Boston University GeneReviews/NIH/NCBI/UW entry on Williams or Williams-Beuren Syndrome The Elastin Protein Microfibril This article incorporates...

function during pre- and postnatal life. This gene is deleted in Williams-Beuren syndrome, a neurodevelopmental disorder affecting multiple systems. Claudin...

Abhydrolase domain-containing protein 11 also known as Williams-Beuren syndrome chromosomal region 21 protein (WBSCR21) is an enzyme that in humans is...

Ballabio A, Reymond A (March 2001). "WBSCR14, a gene mapping to the Williams--Beuren syndrome deleted region, is a new member of the Mlx transcription factor...

This gene is located at chromosome 7p13 which is close to the Williams Beuren syndrome chromosome region 7q11.23. GRCh38: Ensembl release 89: ENSG00000136206...

transcriptional and epigenetic dysfunctions in Williams Beuren syndrome and 7q11.23 microduplication syndrome, following their seminal work published in Nature...

same genes that are missing in individuals with Williams-Beuren syndrome. Also so called XYY syndrome can often cause speech delay. Twins Being a twin...

chromatin-dependent regulation of transcription. This gene is deleted in Williams-Beuren syndrome, a developmental disorder caused by deletion of multiple genes...

"Characterization of two novel genes, WBSCR20 and WBSCR22, deleted in Williams-Beuren syndrome". Cytogenet Cell Genet. 95 (1–2): 20–7. doi:10.1159/000057012....

(December 2000). "Structure of the PHD zinc finger from human Williams-Beuren syndrome transcription factor". Journal of Molecular Biology. 304 (5): 723–9...

Clarkson, Patricia M.; Berdon, Walter E. (2010). "John C. P. Williams of Williams-Beuren syndrome". Pediatric Radiology. 41 (2): 267–269. doi:10.1007/s00247-010-1909-y...

neurodegenerative disorders include Rett syndrome, Prader–Willi syndrome, Angelman syndrome, and Williams-Beuren syndrome. Neurogenetics Comparative genomics...