Clinical Manifestations and Molecular Investigation of 50 Patients with Williams Syndrome in the Greek Population-Reference-Cited by-同舟云学术

Clinical Manifestations and Molecular Investigation of 50 Patients with Williams Syndrome in the Greek Population

Published:2005-06 Issue:6 Volume:57 Page:789-795
ISSN:0031-3998
Container-title:Pediatric Research
language:
Short-container-title:Pediatr Res

Author:

Amenta Stella,Sofocleous Christalena,Kolialexi Angeliki,Thomaidis Loretta,Giouroukos Sotiris,Karavitakis Emmanuel,Mavrou Ariadni,Kitsiou Sophia,Kanavakis Emmanuel,Fryssira Helen

Publisher

Springer Science and Business Media LLC

Subject

Pediatrics, Perinatology and Child Health

Reference74 articles.

1. Supravalvular Aortic Stenosis

2. Familial Williams-Beuren syndrome showing varying clinical expression

3. The elastin gene is disrupted in a family with a balanced translocation t(7;16)(q11.23;q13) associated with a variable expression of the Williams-Beuren syndrome

4. Williams syndrome: Autosomal dominant inheritance

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