Alpha 1 antitrypsin deficiency alleles are associated with joint dislocation and scoliosis in Williams syndrome
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajmg.c.30265/fullpdf
Reference29 articles.
1. Segregation of a novel FBN1 gene mutation, G1796E, with kyphoscoliosis and radiographic evidence of vertebral dysplasia in three generations;Ades;Am J Med Genet,2002
2. Approximate is better than “Exact” for interval estimation of binomial proportions;Agresti;Am Stat,1998
3. Adolescent idiopathic scoliosis: Natural history and long term treatment effects;Asher;Scoliosis,2006
4. Association between IL-6 and MMP-3 gene polymorphisms and adolescent idiopathic scoliosis;Aulisa;Spine,2007
5. Pediatric hernias;Brandt;Surg Clin North Am,2008
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