Author:
Nucaro A,Pisano T,Chillotti I,Montaldo C,Pruna D
Subject
Genetics (clinical),Genetics
Reference6 articles.
1. Identification and molecular characterization of two novel chromosomal deletions associated with autism.;Chien;Clin Genet,2010
2. Two patients with balanced translocations and autistic disorder: CSMD3 as a candidate gene for autism found in their common 8q23 breakpoint area.;Floris;Eur J Hum Genet,2008
3. A novel giant gene CSMD3 encoding a protein with CUB and sushi multiple domains: a candidate gene for benign adult familial myoclonic epilepsy on human chromosome 8q23.3-q24.1.;Shimizu;BBRC,2003
4. CSMD1 is a novel multiple domain complement-regulatory protein highly expressed in the central nervous system and epithelial tissues.;Kraus;J Immunol,2006
5. Transmitted duplication of 8p23.1-8p23.2 associated with speech delay, autism and learning difficulties.;Glancy;Eur J Hum Genet,2009
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