Partial monosomy 12p13.1----13.3.
Open Access
- 1 July 1987
- journal article
- case report
- Published by BMJ in Journal of Medical Genetics
- Vol. 24 (7) , 434-436
- https://doi.org/10.1136/jmg.24.7.434
Abstract
We describe a 27 month old female child with partial monosomy for the short arm of chromosome 12: 46,XX,del(12)(p13.1----p13.3). She differs from the eight cases described by others, in that she is less severely affected. Her main clinical features are developmental delay, protruding tongue, strabismus, slightly unusual facies, slight micrognathia, and speech delay.Keywords
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