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Browsing by Author Bruno, D.L.
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Author(s)
2009
Extending the phenotype of recurrent rearrangements of 16p11.2: deletions in mentally retarded patients without autism and in normal individuals.
Bijlsma, E.K.
;
Gijsbers, A.C.
;
Schuurs-Hoeijmakers, J.H.M.
, et al
2010
Further molecular and clinical delineation of co-locating 17p13.3 microdeletions and microduplications that show distinctive phenotypes.
Bruno, D.L.
;
Anderlid, B.M.
;
Lindstrand, A.
, et al
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