## Abstract This is the first reported case of dystonia with a partial deletion of the long arm (q) of chromosome 18. Neurologic findings in the 18q‐ syndrome include mental retardation, seizures, nystagmus, incoordination, tremor, and chorea. A 36‐year‐old woman with an 18q terminal deletion [Kary
Molecular mapping of a Yq deletion in a patient with normal stature
✍ Scribed by R. Rousseaux-Prévost; Jean-Marc Rigot; Bruno Delobel; Paul Lesur; Francis Collier; Marie-Françoise Croquette; Alain Gauthier; Etienne Mazeman; Jean Rousseaux
- Publisher
- Springer
- Year
- 1996
- Tongue
- English
- Weight
- 20 KB
- Volume
- 98
- Category
- Article
- ISSN
- 0340-6717
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