Abstract
We describe a reciprocal translocation (10;13) in a man, ascertained through the study of meiosis in semen, and a partial trisomy 10q in his abnormal son. The phenotypic anomalies of the partial 10q trisomy syndrome are probably due to the presence in triplicate of the region q25→qter of chromosome 10. © 1980 Springer-Verlag.
Original language | English |
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Pages (from-to) | 179-182 |
Journal | Human Genetics |
Volume | 53 |
DOIs | |
Publication status | Published - 1 Feb 1980 |