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

Bonaglia, MC (author)
Giorda, R (author)
Mani, E (author)
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Aceti, G (author)
Anderlid, BM (author)
Karolinska Institutet
Baroncini, A (author)
Pramparo, T (author)
Zuffardi, O (author)
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 (creator_code:org_t)
2006-03-29
2006
English.
In: Journal of medical genetics. - : BMJ. - 1468-6244. ; 43:10, s. 822-828
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