22q13.3 deletion syndrome: A recognizable malformation syndrome associated with marked speech and language delay
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Reference38 articles.
1. FISH-mapping of a 100-kb terminal 22q13 deletion
2. Unusual dicentric chromosome 22 associated with a 22q13 deletion
3. 22q13 deletion syndrome with central diabetes insipidus: a previously unreported association
4. Characterization of the phenotype and definition of the deletion in a new patient with ring chromosome 22
5. Disruption of the ProSAP2 Gene in a t(12;22)(q24.1;q13.3) Is Associated with the 22q13.3 Deletion Syndrome
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