A NOTE ON A PATIENT WITH A RING-22 CHROMOSOME IDENTIFIED BY BANDING
β Scribed by A. STEWART; B. W. RICHARDS
- Book ID
- 114739844
- Publisher
- John Wiley and Sons
- Year
- 2008
- Tongue
- English
- Weight
- 786 KB
- Volume
- 20
- Category
- Article
- ISSN
- 0964-2633
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
We report on a patient with multiple congenital anomalies and ring chromosome 22 who died at age 16 years of bronchopneumonia. Autopsy documented multiple psammomatous meningiomas of the spinal dura and tentorium. n m o r tissue for cytogenetic analysis was not available. Although abnormalities of c
## To the Editor: The Opitz or BBBG syndrome is an autosomal dominant disorder characterized by facial anomalies and multiple congenital abnormalities. Recent evidence would suggest that the Opitz and BBB syndromes form a spectrum of the same condition Verloes et al., 19891 and it has been sugges