DOI:
10.1055/s-00029027
Journal of Pediatric Genetics
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References
Benito-Sanz S, Royo JL, Barroso E. , et al.
Identification of the first recurrent PAR1 deletion in Léri-Weill dyschondrosteosis and idiopathic short stature reveals the presence of a novel SHOX enhancer.
J Med Genet 2012;
49 (07) 442-450
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