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On the syndrome caused by a deletion of the short arm of a 4-5 chromosome
Published online by Cambridge University Press: 01 August 2014
Summary
During routine karyotypic analysis of patients with mental deficiency and congenital malformations, a partial deletion of the short arm of a B (4-5) chromosome was observed in two children (a male, 23 months old, and a female, 4 months old).
Clinical pictures and chromosomal abnormalities were found to be consistent with the findings in the « cri du chat » syndrome.
- Type
- Research Article
- Information
- Acta geneticae medicae et gemellologiae: twin research , Volume 15 , Issue 1 , January 1966 , pp. 36 - 50
- Copyright
- Copyright © The International Society for Twin Studies 1966
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