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.
| Autor: | Behjati F; Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran. f_behjati@uswr.ac.ir, Shafeghati Y, Kahrizi K, Firouzabadi SG, Najmabadi H, Dixon N, Davies AF |
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| Jazyk: | angličtina |
| Zdroj: | American journal of medical genetics. Part A [Am J Med Genet A] 2008 Dec 15; Vol. 146A (24), pp. 3223-6. |
| DOI: | 10.1002/ajmg.a.32575 |
| Databáze: | MEDLINE |
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