Malformations among the X-linked intellectual disability syndromes
Author:
Affiliation:
1. Greenwood Genetic Center; Greenwood South Carolina
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Reference26 articles.
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2. Mutations in the chromatin-associated protein ATRX;Gibbons;Hum Mutat,2008
3. Doublecortin, a brain specific gene mutated in human X-linked lissencephaly and double cortex syndrome, encodes a putative signaling protein;Gleeson;Cell,1998
4. Long term survival in TARP syndrome and confirmation of RBM10 as the disease causing gene;Gripp;Am J Med Genet Part A,2011
5. Familial occurrence of the VATER/VACTERL association;Hilger;Pediatr Surg Int,2012
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