IL1RAPL1 gene deletion as a cause of X-linked intellectual disability and dysmorphic features
Author:
Publisher
Elsevier BV
Subject
Genetics (clinical),Genetics,General Medicine
Reference22 articles.
1. Novel mutation of IL1RAPL1 gene in a nonspecific X-linked mental retardation (MRX) family;Nawara;Am. J. Med. Genet. Part A,2008
2. Nonspecific X-linked mental retardation II: the frequency in British Columbia;Herbst;Am. J. Med. Genet.,1980
3. XLMR genes: update 2000;Chiurazzi;Eur. J. Med. Genet.,2001
4. Fragile X and X-linked mental retardation;Jacquemont,2005
5. FMR1 and fragile X syndrome: human genome epidemiology review;Crawford;Genet. Med.,2001
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