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Last Updated: 06/20/2022

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Found 18 publications

Oxytocin and Oxytocin Receptor Gene Regulation in Williams Syndrome: A Systematic Review.

Midaortic syndrome and renovascular hypertension.

Efficacy of denosumab therapy for a 12-year-old female patient with Williams syndrome with osteoporosis and history of fractures: a case report.

Nationwide questionnaire data of 229 Williams-Beuren syndrome patients using WhatsApp tool.

Revealing Chronic Granulomatous Disease in a Patient With Williams-Beuren Syndrome Using Whole Exome Sequencing.

Coronary artery patch augmentation for congenital left coronary ostial stenosis in Williams syndrome.

Compound Heterozygote of Point Mutation and Chromosomal Microdeletion Involving OTUD6B Coinciding with ZMIZ1 Variant in Syndromic Intellectual Disability.

Autism Spectrum Disorders: Analysis of Mobile Elements at 7q11.23 Williams-Beuren Region by Comparative Genomics.

Hybrid Left Heart Bypass Circuit for Repair of the Descending Aorta in an 8-kg Williams Syndrome Patient.

Motion perception and its disorders.

Hashimoto's Thyroiditis and Graves' Disease in Genetic Syndromes in Pediatric Age.

Mid-Aortic Syndrome in Williams-Beuren Syndrome with an Atypical Small-Sized Deletion of Chromosome 7q11.23 Misdiagnosed as Takayasu Arteritis.

Showing 1-12 of 18

Last Updated: 06/20/2022