Facial phenotype at different ages and cardiovascular malformations in children with Williams-Beuren syndrome: A study from India
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajmg.a.35443/fullpdf
Reference20 articles.
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2. Williams syndrome: Pediatirc, neurologic and cognitive development;Carrasco;Pediatr Neurol,2005
3. Cardiovascular abnormalities, interventions, and long-term outcomes in infantile Williams syndrome;Collins;J Pediatr,2010
4. Hemizygosity at the NCF1 gene in patients with Williams-Beuren syndrome decreases their risk of hypertension;Del Campo;Am J Hum Genet,2006
5. Cardiovascular manifestations in 75 patients with Williams syndrome;Eronen;J Med Genet,2002
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4. Objective differential diagnosis of Noonan and Williams–Beuren syndromes in diverse populations using quantitative facial phenotyping;Molecular Genetics & Genomic Medicine;2021-03-27
5. Assessment of Multiplex Ligation-Dependent Probe Amplification (MLPA) as a diagnostic test for Egyptian patients with Williams-Beuren syndrome;Gene Reports;2020-09
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