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 (Journal Indexed in SCI) identifier identifier identifier

  • Publication Type: Article / Article
  • Volume:
  • Publication Date: 2011
  • Doi Number: 10.1002/ajmg.a.34101
  • Title of Journal : American journal of medical genetics. Part A
  • Page Numbers: pp.1745-52