|
| Human syndrome | Associated genetic change | Aneuploid mouse models |
|
| Angelman syndrome | deletion of maternal 15q11–13 | PatDp [37] |
| MatDf(Ube3a-Gabrb3) [38] |
| Prader-Willi syndrome | deletion of paternal 15q11–13 | MatDp [37] |
| Autism risk factor | Duplication 15q11–13 | matDp; pat Dp [57] |
| Smith-Magenis syndrome | deletion of 17p11/17p11.2 | Df(11)17 [58] |
| Df(11)17-1; Df(11)17-2; Df(11)17-3 [59] |
| Potocki-Lupski syndrome | duplication of 17p11/17p11.2 | Dp(11)17 [58] |
| DiGeorge syndrome | deletion of 22q11.2 | Df1 [44] |
| Idd-Ctp [45] |
| Idd-Arvcf [46] |
| Df2; Df3; Df4; Df5 [60] |
| Williams-Beuren | deletion of 7q11 | PD and DD [53] |
| — | deletion/duplication of 17q21 | Df11[
1] and Dp11[ 1] [35] |
|