Cytogenetic analysis of an extraskeletal myxoid chondrosarcoma revealed a der(16)t(1;16)(q21;q13) in addition to the t(9;22)(q22;q12) described as characteristic for this chondrosarcoma clinicohistopathologic subtype. An identical der( 16) has been identified as the most common secondary structural
der(16)t(1;16)(q21;q13) as a secondary change in Alveolar Rhabdomyosarcoma: A case report and review of the literature
β Scribed by Aidan P. McManus; Toon Min; G. John Swansbury; Barry A. Gusterson; C. Ross Pinkerton; Janet M. Shipley
- Book ID
- 113253691
- Publisher
- Elsevier Science
- Year
- 1996
- Tongue
- English
- Weight
- 290 KB
- Volume
- 87
- Category
- Article
- ISSN
- 0165-4608
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
## Abstract An infant with multiple congenital anomalies and severe developmental delay was found to have a derivative chromosome 4 by routine karyotypic analysis. Using telomeric FISH analysis, the source of the additional chromatin was determined to be from 20q. The infant, thus, is trisomic for
We report on a case of dup(l6p) and review previous cases. The triplicated chromosome region leading to this specific syndrome lies in 16~13.1 p13.3. Most of the cases are inherited and the mode of segregation was found to be 3: 1 in half of the cases, but these observations might be due to biases.