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Identification of a recurrent brerakpoint within the SHANK3 gene in the 22q13.3 deletion syndrome.

Academic Article
Publication Date:
2006
Iris type:
1.1 Articolo in rivista
Keywords:
array CGH; epilessia deletion syndrome
List of contributors:
Bonaglia, Mc; Pramparo, Tiziano; Mani, E; Aceti, G; Anderlid, Bm; Baroncini, A; Pramparo, T.
Handle:
https://iris.unipv.it/handle/11571/381304
Published in:
JOURNAL OF MEDICAL GENETICS
Journal
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