| 1 | ACLS4, DELXQM
|
| Xq22.3-q23 deletion including ACSL4 in a patient with intellectual disability.
|
| Gazou A, Riess A, Grasshoff U, Schäferhoff K, Bonin M, Jauch A, Riess O, Tzschach A.
|
| Am J Med Genet A 161(4):860-4. doi: 10.1002/ajmg.a.35778. Epub 2013 Mar 12.
2013
|
| 2 | AFF2, DELXQM, FRAXE
|
| Microdeletion of Xq28 involving the AFF2 (FMR2) gene in two unrelated males with developmental delay.
|
| Sahoo T, Theisen A, Marble M, Tervo R, Rosenfeld JA, Torchia BS, Shaffer LG.
|
| Am J Med Genet A 155(12):3110-5. doi: 10.1002/ajmg.a.34345. Epub 2011 Nov 7. 2011
|
| 3 | DELXQM, MRXS30, UBE2A
|
| Novel deletion at Xq24 including the UBE2A gene in a patient with X-linked mental retardation.
|
| Honda S, Orii KO, Kobayashi J, Hayashi S, Imamura A, Imoto I, Nakagawa E, Goto Y, Inazawa J.
|
| J Hum Genet 55(4):244-7. Epub 2010 Mar 26. 2010
|