Abstract
We report on three patients with duplication of distal 22q. One patient is a de novo carrier of the translocation t(21;22) (p13;q11), the other two are offspring of a translocation carrier t(10;22) (q26;q12). The clinical manifestations of these patients demonstrate the variability to the dup(22q) syndrome.
Original language | English |
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Pages (from-to) | 346-349 |
Number of pages | 4 |
Journal | American Journal of Medical Genetics |
Volume | 32 |
Issue number | 3 |
DOIs | |
State | Published - 1 Jan 1989 |
ASJC Scopus subject areas
- Genetics(clinical)