This report describes the fourth case of heritable 18p monosomy, which was ascertained by prenatal diagnosis. Cytogenetic analysis of amniotic Β―uid cells by G-banding showed an apparently distal 18p chromosome deletion and a derivative X chromosome resulting from a translocation between the X and Y
18p trisomy: A case of direct 18p duplication characterized by molecular cytogenetic analysis
β Scribed by H. Marical; M.J. Le Bris; N. Douet-Guilbert; P. Parent; J.P. Descourt; F. Morel; M. De Braekeleer
- Publisher
- John Wiley and Sons
- Year
- 2007
- Tongue
- English
- Weight
- 79 KB
- Volume
- 143A
- Category
- Article
- ISSN
- 1552-4825
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## Abstract Small supernumerary marker chromosomes (sSMC) have been described from all human chromosomes with different sizes and shapes. However, it is difficult to know the clinical manifestations associated with them, because such knowledge depends on the size, presence of euchromatic material,
Please note that Figure 2A needed correction. [A] FISH using subtelomere probes [TelVysion 2p Spectrum green (VIJyRM2052) and TelVysion 2q Spectrum orange (VIJyRM2123)] from Abbott Molecular. The legend is correct; however, the chromosome on the left should have a red signal designated with q and n