Trisomy 10p due to a de novo t(10p;13p)
- PMID: 422195
- DOI: 10.1007/BF00291912
Trisomy 10p due to a de novo t(10p;13p)
Abstract
A new case of trisomy 10p has been identified by means of the GTG-banding technique. The patient is a female child carrying a sporadic translocation, t(10;13)(p11;p11), and affected by microsomatia and microcephaly with facial dysmorphia, retarded growth, weight gain, and psychomotor development, and bilateral talipes.
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