Abstract
Two patients with partial monosomy of the short arm of chromosome 8 are described. Their clinical features were very similar. Comparison with previously reported patients confirms the existence of an 8p- syndrome. The importance of cytogenetic investigations in all infants with major congenital heart defect and facial dysmorphism or microcephaly or both is stressed.
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CITATION STYLE
APA
Brocker-Vriends, A. H. J. T., Mooij, P. D., van Bel, F., Beverstock, G. C., & van de Kamp, J. J. (1986). Monosomy 8p: An easily overlooked syndrome. Journal of Medical Genetics, 23(2), 153–154. https://doi.org/10.1136/jmg.23.2.153
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