Trisomy 16q13→qter in a infant from a t (11;16)(q25;q13) translocation-carrier father
✍ Scribed by K. Hatanaka; M. Ozaki; M. Suzuki; R. Murata; H. Fujita
- Publisher
- Springer
- Year
- 1984
- Tongue
- English
- Weight
- 807 KB
- Volume
- 65
- Category
- Article
- ISSN
- 0340-6717
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An new type of translocation, t(10;13)(q25;q11), is observed in a phenotypically normal male who was examined for subfertility. The meiotic behavior of the rearranged chromosomes indicates that crossing-over is very frequent in a rather small segment such as the short arm of chromosome 13 and consta
Members of three generations of a single family were examined and found to have a balanced translocation t(11;16)(q13;p11). Cytogenetic investigation and investigation of a number of gene markers is consistent with the current view that the Hp-alpha locus is situated in the proximity of band 16q22.
We describe a female new-born with partial trisomy of the long arm of chromosome 16. The chromosome anomaly was the result of an unbalanced segregation of a maternal translocation t(13;16)(p12;q23). Dynamic (RBG, GBG) banding and the Ag-NOR technique ascertained the reciprocal balanced maternal tran