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: | Angela F. Davies, Farkhondeh Behjati, Hossein Najmabadi, Kimia Kahrizi, Yousef Shafeghati, Saghar Ghasemi Firouzabadi, Neil Dixon |
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| Rok vydání: | 2008 |
| Předmět: |
Adult
Heart Defects Congenital Male Genetics Pathology medicine.medical_specialty Heart disease Chromosomes Human Pair 10 business.industry Chromosome Mapping Chromosome medicine.disease Developmental disorder Intellectual Disability Karyotyping medicine Humans Abnormalities Multiple Female Chromosome Deletion Child business Genetics (clinical) |
| Zdroj: | American Journal of Medical Genetics Part A. :3223-3226 |
| ISSN: | 1552-4833 1552-4825 |
| DOI: | 10.1002/ajmg.a.32575 |
| Databáze: | OpenAIRE |
| Externí odkaz: |
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