Identification of a recurrent breakpoint within the SHANK3 gene in the 22q13.3 deletion syndrome.
Bonaglia, M. C.; Giorda, R.; Mani, E.; Aceti, G.; Anderlid, B.-M.; Baroncini, A.; Pramparo, T.; Zuffard, O.; Journal of Medical Genetics, 2006, vol. 43, issue 10, p 822, ISSN 00222593. ISBN 14686244.

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