Clinical, cytogenetic, and molecular characterization of six patients with ring chromosomes 22, including one with concomitant 22q11.2 deletion
✍ Scribed by Guilherme, Roberta Santos; Soares, Karina Cunha; Simioni, Milena; Vieira, Tarsis Paiva; Gil-da-Silva-Lopes, Vera Lúcia; Kim, Chong Ae; Brunoni, Décio; Spinner, Nancy Bettina; Conlin, Laura Kathleen; Christofolini, Denise Maria; Kulikowski, Leslie Domenici; Steiner, Carlos Eduardo; Melaragno, Maria Isabel
- Book ID
- 121655602
- Publisher
- John Wiley and Sons
- Year
- 2014
- Tongue
- English
- Weight
- 163 KB
- Volume
- 164
- Category
- Article
- ISSN
- 1552-4825
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Malignant rhabdoid tumors are rare and aggressive neoplasms of childhood, occurring in the kidney or in various extrarenal locations. Most cytogenetic studies of these tumors have shown the frequent involvement of chromosome 22, including translocations and/or deletions, with a critical region for a