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...

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

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

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...

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

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...

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

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

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

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

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...

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

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...

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

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...

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

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...

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...

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

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....

transcription factor gene (WBSCR11) that is commonly deleted in Williams-Beuren syndrome". Genomics. 57 (2): 279–84. doi:10.1006/geno.1999.5784. PMID 10198167...

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