Molecular cytogenetic analysis of a familial 8p23.1 deletion associated with minimal dysmorphic features, seizures, and mild mental retardation
- 1 August 1992
- journal article
- case report
- Published by Springer Nature in Human Genetics
- Vol. 89 (6), 602-606
- https://doi.org/10.1007/bf00221946
Abstract
No abstract availableKeywords
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