A 10.46 Mb 12p11.1-12.1 interstitial deletion coincident with a 0.19 Mb NRXN1 deletion detected by array CGH in a girl with scoliosis and autism.


SOYSAL Y., VERMEESCH J., DAVANI N., Hekimler K., IMIRZALIOĞLU N.

American journal of medical genetics. Part A, pp.1745-52, 2011 (SCI-Expanded) identifier identifier identifier