Inversion of ‘fluorescent’ segment in chromosome 3: A polymorphic trait
✍ Scribed by D. Soudek; Helena Sroka
- Publisher
- Springer
- Year
- 1978
- Tongue
- English
- Weight
- 346 KB
- Volume
- 44
- Category
- Article
- ISSN
- 0340-6717
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✦ Synopsis
The frequency of the 'inversion' of flourescent constitutive heterochromatin in chromosome 3 was the same in a sample of 370 retarded persons as in a sample of 222 mentally normal men. It can be concluded that this 'inversion' is not associated with mental retardation. This variant is more common (4%) in the Canadian population we studied than in samples reported by most other authors (0-1.7%). Possibly the founder effect could play a role in the differences. Two cases of homozygotes for this 'inversion' were identified.
📜 SIMILAR VOLUMES
We report the prenatal exclusion of partial trisomy in a family with maternal pericentric inversion of chromosome 21 by fluorescence in situ hybridization (FISH). After determining the structural rearrangement in the mother and her affected son with 46,XY,rec(21)dup(21q)inv(21)(p11q22) resulting in