A child with nasal hypoplasia, growth and developmental delay, and 18p--due to 14q/18q apparent dicentric fusion is reported. Review of ten previously reported patients with 18p--due to fusion translocations involving the long arm of chromosome 18 reveals clinical features ranging from arrhinencepha
β¦ LIBER β¦
18q- Syndrome resulting from a tdic(14p;18q)
β Scribed by J. C. Lambert; Martine Ferrari; C. Bergondi; Alena Galliana; N. Ayraud
- Book ID
- 104696808
- Publisher
- Springer
- Year
- 1979
- Tongue
- English
- Weight
- 572 KB
- Volume
- 48
- Category
- Article
- ISSN
- 0340-6717
No coin nor oath required. For personal study only.
β¦ Synopsis
A case of 18q- syndrome due to a de novo tdic(14p;18q) is presented. The interest of this observation lies in the rarity of stable dicentric chromosomes arising from reciprocal translocations between autosomes.
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