Back to search

Article

Autism in patients with Williams-Beuren syndrome: A re-evaluation of 31 Tunisian patients’ phenotype

2022-10-17

Abstract excerpt

<h4>Background: </h4> Williams Beuren Syndrome is a multisystemic disorder manifested by congenital heart defects associated with dysmorphic features, intellectual delay, and a particular behavioural profile due to a microdeletion in 7q11.2. Methods To establish a genotype-phenotype correlation; we carried out a molecular cytogenetic analysis on 31 Tunisian WBS patients using the CGH-array and FISH techniques. Re...

Topics

Open a Topic to create a Post that cites this publication.

Identifiers and source

Literature Corpus work
b5dab3ab-6940-56c8-af4a-80fe71fad9b9
DOI
10.21203/rs.3.rs-2139963/v1
Open publication

Related research

Semantic proximity does not establish scientific evidence.

Click a neighbor to travelStep 1 · 12 closest
Interactive article relationship graphSelect a related publication card to move it into the centre and load its closest explainable connections. Solid lines are source-backed structured connections. Dashed lines are semantic discovery signals and are not scientific evidence.
Autism in patients with Williams-Beuren syndrome: A re-evaluation of 31 Tunisian patients’ phenotypeDOI 10.21203/rs.3.rs-2139963/v1
Select a neighboring publication to make it the new centre.