A t(13q14q) family with the translocation and a Philadelphia chromosome in one member
✍ Scribed by Johan Wennström; Jim Schröder
- Publisher
- Springer
- Year
- 1973
- Tongue
- English
- Weight
- 230 KB
- Volume
- 20
- Category
- Article
- ISSN
- 0340-6717
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## Abstract Cytogenetic studies of a rhabdomyosarcoma of mixed embryonal and alveolar histology in an II ‐month‐old male revealed a single structural abnormality, t(1;13)(p36;q14). This abnormality may define a subset of patients with a variant of the t(2;13)(q35;q14) translocation frequently seen
We present a 6-year-old girl with a balanced 11;20 translocation [46,XX,t(11;20)(q13.1; q13.13)patl, asplenia, pulmonic stenosis, Hirschsprung disease, minor anomalies, and mental retardation. This case represents the second report of an individual with situs abnormalities and a balanced chromosome
A case of an inherited type of D/G translocation D1-trisomy syndrome was described. A female proposita who had the clinical signs of D1-trisomy syndrome was found to have a chromosome complement of 46,XX,--G,+t(DqGq). examination of Q- and G-stained karyotypes revealed that the chromosomes involved