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Variability of r(22) Chromosome Phenotypical Expression
Published online by Cambridge University Press: 26 February 2025
Abstract
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Two unrelated patients with multiple congenital malformations and severe mental retardation were found to be carrier of a non-mosaic ring 22 chromosome abnormality. These observations further confirm the phenotypical variability of r(22) expression, which makes unreliable the attempts to delineate a clinical profile of the syndrome
- Type
- Brief Report
- Information
- Acta geneticae medicae et gemellologiae: twin research , Volume 26 , Issue 3-4 , October 1977 , pp. 287 - 290
- Copyright
- Copyright © The International Society for Twin Studies 1977
References
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