Trisomy 10p syndrome owing to maternal pericentric inversion.
review · Level V
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- Record sourced from PubMed, PMID 2182876.
- Also identified by PMC identifier 1017032.
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Abstract
A female infant with karyotype 46,XX,rec(10),dup p inv(10)(p11.2q25.2)mat is presented. She had both duplication of 10p and deletion of distal 10q, but only had the constellation of specific features characteristic of duplication of 10p.
Medical subject headings
- Chromosome Inversion
- Chromosomes, Human, Pair 10
- Trisomy