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Research Letter

Interstitial deletion of the short arm of chromosome 10 del(10)(p11.2p12.32) in a patient with congenital heart disease, minor dysmorphism, and mental retardation†

  1. Farkhondeh Behjati1,*,
  2. Yousef Shafeghati1,
  3. Kimia Kahrizi1,
  4. Saghar Ghasemi Firouzabadi1,
  5. Hossein Najmabadi1,
  6. Neil Dixon2,
  7. Angela F. Davies2

Article first published online: 14 NOV 2008

DOI: 10.1002/ajmg.a.32575

Issue

American Journal of Medical Genetics Part A

American Journal of Medical Genetics Part A

Volume 146A, Issue 24, pages 3223–3226, 15 December 2008

Additional Information

How to Cite

Behjati, F., Shafeghati, Y., Kahrizi, K., Firouzabadi, S. G., Najmabadi, H., Dixon, N. and Davies, A. F. (2008), Interstitial deletion of the short arm of chromosome 10 del(10)(p11.2p12.32) in a patient with congenital heart disease, minor dysmorphism, and mental retardation. Am. J. Med. Genet., 146A: 3223–3226. doi: 10.1002/ajmg.a.32575

Author Information

  1. 1

    Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran

  2. 2

    Cytogenetics Department, Guy's & St. Thomas's Hospital Trust, London, UK

*Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Evin, Koodakyar St., Tehran 19834, Iran.

  1. †

    How to cite this article: Behjati F, Shafeghati Y, Kahrizi K, Firouzabadi SG, Najmabadi H, Dixon N, Davies AF. 2008. Interstitial deletion of the short arm of chromosome 10 del(10)(p11.2p12.32) in a patient with congenital heart disease, minor dysmorphism, and mental, retardation. Am J Med Genet Part A 146A:3223–3226.

Publication History

  1. Issue published online: 21 NOV 2008
  2. Article first published online: 14 NOV 2008
  3. Manuscript Accepted: 8 AUG 2008
  4. Manuscript Received: 19 MAR 2008

Funded by

  • German Human Genome project. Grant Number: 01KW99087

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