We report on a newborn girl with multiple congenital anomalies, whose G-banded chromosome analysis showed complete trisomy 22. Chromosome painting using a whole-chromosome painting probe for chromosome 22 confirmed that neither chromosome 22 was involved in a cryptic translocation.
Partial trisomy 13q identified by sequential fluorescence in situ hybridization
β Scribed by Rao, V. V. N. Gopal ;Carpenter, Nancy J. ;Gucsavas, Muge ;Coldwell, James ;Say, Burhan
- Publisher
- John Wiley and Sons
- Year
- 1995
- Tongue
- English
- Weight
- 365 KB
- Volume
- 58
- Category
- Article
- ISSN
- 0148-7299
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