17q21.31 Microdeletion associated with infantile spasms
Author:
Publisher
Elsevier BV
Subject
Genetics (clinical),Genetics,General Medicine
Reference33 articles.
1. 17q21.31 microdeletion syndrome;Koolen,2012
2. A 17q21.31 microdeletion encompassing the MAPT gene in a mentally impaired patient;Varela;Cytogenet. Genome Res.,2006
3. Clinical and molecular delineation of the 17q21.31 microdeletion syndrome;Koolen;J. Med. Genet.,2008
4. A new chromosome 17q21.31 microdeletion syndrome associated with a common inversion polymorphism;Koolen;Nat. Genet.,2006
5. Discovery of previously unidentified genomic disorders from the duplication architecture of the human genome;Sharp;Nat. Genet.,2006
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