Summary
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.
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Miró, R., Templado, C., Ponsá, M. et al. Balanced translocation (10;13) in a father, ascertained through the study of meiosis in semen, and partial trisomy 10q in his son. Hum Genet 53, 179–182 (1980). https://doi.org/10.1007/BF00273492
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DOI: https://doi.org/10.1007/BF00273492