Follow-up of 16q deletions
β Scribed by Fryns, Jean-Pierre
- Publisher
- John Wiley and Sons
- Year
- 1990
- Tongue
- English
- Weight
- 59 KB
- Volume
- 37
- Category
- Article
- ISSN
- 0148-7299
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π SIMILAR VOLUMES
Partial deletion of 16q is rare; to our knowledge only 12 cases have been published
The most commonly reported manifestations of 16q deletions are severe growth and developmental disorders and anomalies of the craniofacial, visceral, and musculoskeletal systems. We reviewed the findings of patients reported with 16q-syndrome and compared them to our patient, a 4 1 β2-yearold boy wi
We read with interest the paper by Leana-Cox et al. [1996] which reported on 5 families with recurrent Di-George/velocardiofacial syndrome and deletions of chromosome 22q11 (del22q11), and which reviewed the pertinent literature. The authors observed that up to 25% of del22q11 are inherited. Particu