## Abstract Interstitial deletions of the proximal long arm of chromosome 3 are very rare and a defined clinical phenotype is not established yet. We report on the clinical, cytogenetic and molecular findings of a 20βmonthβold Hispanic male with a 2.5 Mb de novo deletion on q13.11q13.12. Up to now,
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Further delineation of the dup(3q) syndrome
β Scribed by Wilson, Golder N. ;Dasouki, Majed ;Barr, Mason ;Opitz, John M. ;Reynolds, James F.
- Publisher
- John Wiley and Sons
- Year
- 1985
- Tongue
- English
- Weight
- 499 KB
- Volume
- 22
- Category
- Article
- ISSN
- 0148-7299
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