Deletion 1q43 encompassing only CHRM3 in a patient with autistic disorder
Author:
Publisher
Elsevier BV
Subject
Genetics(clinical),Genetics,General Medicine
Reference12 articles.
1. High-resolution array CGH defines critical regions and candidate genes for microcephaly, abnormalities of the corpus callosum, and seizure phenotypes in patients with microdeletions of 1q43q44;Ballif;Hum. Genet.,2012
2. Subtelomeric deletions of 1q43q44 and severe brain impairment associated with delayed myelination;Shimojima;J. Hum. Genet.,2012
3. FISH and cytogenetic characterization of a terminal chromosome 1q deletion: clinical case report and phenotypic implications;Gentile;Am. J. Med. Genet.,2003
4. Association of terminal chromosome 1 deletion with Sertoli cell-only syndrome;Hathout;Am. J. Med. Genet.,1998
5. De novo 911 kb interstitial deletion on chromosome 1q43 in a boy with mental retardation and short stature;Perrone;Eur. J. Med. Genet.,2012
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