Medical Overview And Genetics Of Williams Beuren Syndrome

Williams Syndrome, Williams Beuren Syndrome: …

https://my.clevelandclinic.org/health/diseases/15174-williams-syndrome

Williams syndrome, also known as Williams-Beuren syndrome, is a rare, neurodevelopmental, genetic condition characterized by many symptoms including unique physical features, delayed development, cognitive challenges and …

Medical overview and genetics of Williams-Beuren …

https://www.sciencedirect.com/science/article/abs/pii/S1058981305000354

Williams Syndrome - National Organization for Rare …

https://rarediseases.org/rare-diseases/williams-syndrome/

Medical overview and genetics of Williams-Beuren …

https://www.semanticscholar.org/paper/Medical-overview-and-genetics-of-Williams-Beuren-Smoot-Zhang/07e2081cb9c6e40eb4f393e92295f6f87f3cffb2

Medical overview and genetics of Williams-Beuren syndrome @article{Smoot2005MedicalOA, title={Medical overview and genetics of Williams …

Williams–Beuren Syndrome | NEJM

https://www.nejm.org/doi/full/10.1056/NEJMra0903074

Williams–Beuren syndrome, a multisystem disorder caused by the deletion of a chromosome region of 1.5 million to 1.8 million base …

The genomic basis of the Williams-Beuren syndrome

https://pubmed.ncbi.nlm.nih.gov/19039520/

The Williams-Beuren syndrome is a genomic disorder (prevalence: 1/7,500 to 1/20,000), caused by a hemizygous contiguous gene deletion on chromosome 7q11.23. Typical …

Williams syndrome: MedlinePlus Genetics

https://medlineplus.gov/genetics/condition/williams-syndrome/

Description. Williams syndrome is a developmental disorder that affects many parts of the body. This condition is characterized by mild to moderate intellectual disability or learning problems, unique …

Medical overview and genetics of Williams-Beuren …

https://www.academia.edu/13879708/Medical_overview_and_genetics_of_Williams_Beuren_syndrome

Williams-Beuren syndrome (WBS) is a multisystem genetic disorder caused by a microdeletion on chromosome 7. The majority of patients demonstrate cardiovascular …

Williams-Beuren syndrome: genes and mechanisms

https://pubmed.ncbi.nlm.nih.gov/10469848/

Williams-Beuren syndrome (WBS; OMIM 194050) is caused by heterozygous deletions of approximately 1.6 Mb of chromosomal sub-band 7q11.23. The deletions are rather …

Williams–Beuren Syndrome: A Complete Guide For Oral Healthcare

https://williams-syndrome.org/resources/medical-journal-article/williams-beuren-syndrome-a-complete-guide-for-oral-healthcare

Introduction: Williams–Beuren syndrome is a rare, congenital, multisystem disorder, resulting from genetic alterations on chromosome 7q11.23. Characteristic features of …