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| Shinawi M, Sahoo T, Maranda B, et al. (2011) 11p14.1 microdeletions associated with ADHD, autism, developmental delay, and obesity. American Journal of Medical Genetics. Part A. 155: 1272-80 |
| Nagamani SCS, Erez A, Eng C, et al. (2009) Interstitial deletion of 6q25.2-q25.3: A novel microdeletion syndrome associated with microcephaly, developmental delay, dysmorphic features and hearing loss European Journal of Human Genetics. 17: 573-581 |
| Brunetti-Pierri N, Sahoo T, Frioux S, et al. (2008) 15q13q14 deletions: phenotypic characterization and molecular delineation by comparative genomic hybridization. American Journal of Medical Genetics Part A. 146: 1933-1941 |
| Ross MT, Grafham DV, Coffey AJ, et al. (2005) The DNA sequence of the human X chromosome. Nature. 434: 325-37 |