1 El-Fishawy P, "The genetics of autism: key issues, recent findings, and clinical implications" 33 : 83-105, 2010
2 Manning MA, "Terminal 22q deletion syndrome: a newly recognized cause of speech and language disability in the autism spectrum" 114 : 451-457, 2004
3 Luciani JJ, "Telomeric 22q13 deletions resulting from rings, simple deletions, and translocations: cytogenetic, molecular, and clinical analyses of 32 new observations" 40 : 690-696, 2003
4 Philippe A, "Neurobehavioral profile and brain imaging study of the 22q13.3 deletion syndrome in childhood" 122 : e376-e382, 2008
5 Wilson HL, "Molecular characterisation of the 22q13 deletion syndrome supports the role of haploinsufficiency of SHANK3/PROSAP2 in the major neurological symptoms" 40 : 575-584, 2003
6 Bonaglia MC, "Identification of a recurrent breakpoint within the SHANK3 gene in the 22q13.3 deletion syndrome" 43 : 822-828, 2006
7 Bonaglia MC, "Disruption of the ProSAP2 gene in a t(12;22) (q24.1;q13.3) is associated with the 22q 13.3 deletion syndrome" 69 : 261-268, 2001
8 Phelan MC, "Deletion 22q13.3 syndrome http://www. ojrd.com/content/3/1/14" Orphanet Journal of Rare Diseases
9 Nesslinger NJ, "Clinical, cytogenetic, and molecular characterization of seven patients with deletions of chromosome 22q 13.3" 54 : 464-472, 1994
10 Phelan MC, "A de novo terminal deletion of 22q" 43 : A118-, 1988
1 El-Fishawy P, "The genetics of autism: key issues, recent findings, and clinical implications" 33 : 83-105, 2010
2 Manning MA, "Terminal 22q deletion syndrome: a newly recognized cause of speech and language disability in the autism spectrum" 114 : 451-457, 2004
3 Luciani JJ, "Telomeric 22q13 deletions resulting from rings, simple deletions, and translocations: cytogenetic, molecular, and clinical analyses of 32 new observations" 40 : 690-696, 2003
4 Philippe A, "Neurobehavioral profile and brain imaging study of the 22q13.3 deletion syndrome in childhood" 122 : e376-e382, 2008
5 Wilson HL, "Molecular characterisation of the 22q13 deletion syndrome supports the role of haploinsufficiency of SHANK3/PROSAP2 in the major neurological symptoms" 40 : 575-584, 2003
6 Bonaglia MC, "Identification of a recurrent breakpoint within the SHANK3 gene in the 22q13.3 deletion syndrome" 43 : 822-828, 2006
7 Bonaglia MC, "Disruption of the ProSAP2 gene in a t(12;22) (q24.1;q13.3) is associated with the 22q 13.3 deletion syndrome" 69 : 261-268, 2001
8 Phelan MC, "Deletion 22q13.3 syndrome http://www. ojrd.com/content/3/1/14" Orphanet Journal of Rare Diseases
9 Nesslinger NJ, "Clinical, cytogenetic, and molecular characterization of seven patients with deletions of chromosome 22q 13.3" 54 : 464-472, 1994
10 Phelan MC, "A de novo terminal deletion of 22q" 43 : A118-, 1988
11 Dhar SU, "22q13.3 deletion syndrome: clinical and molecular analysis using array CGH" 152A : 573-581, 2010
12 Havens JM, "22q13 deletion syndrome: an update and review for the primary pediatrician" 43 : 43-53, 2004
13 Barakat AJ, "22q13 deletion syndrome with central diabetes insipidus: a previously unreported association" 13 : 191-194, 2004
14 Phelan MC, "22q13 deletion syndrome" 101 : 91-99, 2001