We describe an infant with trisomy of (5)(p10p13.1) resulting from a de novo marker chromosome. The marker's origin was identified by chromosome microdissection and reverse in situ hybridization. The clinical findings are compared to those of other partial and complete 5p duplications. This case fur
Trisomy of 5p and marker chromosomes
β Scribed by Froster, U.G. ;Reichenbach, H.
- Publisher
- John Wiley and Sons
- Year
- 2000
- Tongue
- English
- Weight
- 39 KB
- Volume
- 93
- Category
- Article
- ISSN
- 0148-7299
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