16p13 microduplication without CREBBP involvement: Moving toward a phenotype delineation
Author:
Publisher
Elsevier BV
Subject
Genetics (clinical),Genetics,General Medicine
Reference18 articles.
1. Duplication 16p13.3 and the CREBBP gene: confirmation of the phenotype;Demeer;Eur. J. Med. Genet.,2013
2. 16p subtelomeric duplication: a clinically recognizable syndrome;Digilio;Eur. J. Hum. Genet.,2009
3. Divergent origins and concerted expansion of two segmental duplications on chromosome 16;Eichler;J. Hered.,2011
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5. NMDA receptors in clinical neurology: excitatory times ahead;Kalia;Lancet Neurol.,2008
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