Microdeletion 4p16.3 in three unrelated patients with Wolf-Hirschhorn syndrome
β Scribed by Dufke, A.; Seidel, J.; Schöning, M.; Döbler-Neumann, M.; Kelbova, C.; Liehr, T.; Beensen, V.; Backsch, C.; Klein-Vogler, U.; Enders, H.
- Book ID
- 120551298
- Publisher
- S. Karger AG
- Year
- 2000
- Tongue
- French
- Weight
- 160 KB
- Volume
- 91
- Category
- Article
- ISSN
- 1424-8581
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
## Abstract ## BACKGROUND WolfβHirschhorn syndrome (WHS) is a wellβknown genetic condition characterized by typical facial anomalies, midline defects, skeletal anomalies, prenatal and postnatal growth retardation, hypotonia, mental retardation, and seizures. Affected patients with a microdeletion
Chromosome imbalance affecting the short arm of chromosome 4 results in a variety of distinct clinical conditions. Most of them share a number of manifestations, such as mental retardation, microcephaly, pre-and post-natal growth retardation, anteverted and low-set ears, that can be considered as no