Spondyloenchondrodysplasia: Clinical variability in three cases
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajmg.a.30078/fullpdf
Reference10 articles.
1. Possible heterogeneity in spondyloenchondrodysplasia: quadriparesis, basal ganglia calcification, and chondrocyte inclusions;Frydman;Am J Med Genet,1990
2. Spondylometaphyseal dysplasia in two sibs of normal parents;Gustavson;Pediatr Radiol,1978
3. Spondyloenchondromatosis with d-2-hydroxyglutaric aciduria: A report of a second patient with this unusual combination;Honey;Clin Dysmorphol,2003
4. Spodyloenchondrodysplasia;Menger;J Med Genet,1989
5. Multiple chondroma affecting the spine: Spondylo-enchondroplasia and other forms;Sauvegrain;J Radiol,1980
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