## Abstract Polymicrogyria (PMG) is a relatively common malformation of the cortex for which the pathogenesis remains poorly understood. Both acquired and genetic causes are known, and to date more than 70 cases of PMG have been associated with chromosomal abnormalities. Here we report on a 12βyear
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Inv dup(22), del(22)(q11) and r(22) in the father of a child with DiGeorge syndrome
β Scribed by Bergman, Anne; Blennow, Elisabeth
- Book ID
- 110025018
- Publisher
- Nature Publishing Group
- Year
- 2000
- Tongue
- English
- Weight
- 190 KB
- Volume
- 8
- Category
- Article
- ISSN
- 1018-4813
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