Atypical Williams syndrome in an infant with complete atrioventricular canal defect-Reference-Cited by-同舟云学术

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Atypical Williams syndrome in an infant with complete atrioventricular canal defect

Published:2015-08-14 Issue:12 Volume:167 Page:3108-3112
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Ahrens-Nicklas Rebecca C.¹²,Reichert Sara L.³,Zackai Elaine H.¹²,Kaplan Paige B.¹

Affiliation:

1. Section of Metabolic Disease; The Children's Hospital of Philadelphia; Philadelphia Pennsylvania

2. Division of Genetics; The Children's Hospital of Philadelphia; Philadelphia Pennsylvania

3. Center for Fetal Diagnosis and Treatment; The Children's Hospital of Philadelphia; Philadelphia Pennsylvania

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Reference24 articles.

1. Supravalvular aortic stenosis in association with mental retardation and a certain facial appearance;Beuren;Circulation,1962

2. Sudden death in Williams syndrome: Report of ten cases;Bird;J Pediatr,1996

3. Idiopathic hypercalcemia of infancy, with failure to thrive; report of three cases, with a consideration of the possible etiology;Bongiovanni;N Engl J Med,1957

4. Endocardial cushion defect: Further studies of “isolated” versus “syndromic” occurrence;Carmi;Am J Med Genet,1992

5. Cardiovascular disease in Williams syndrome;Collins;Circulation,2013

Cited by 2 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Case Report: Rapid and progressive left ventricular endocardial calcification in an infant with Williams syndrome;Frontiers in Pediatrics;2024-04-08

2. 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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