Two adjacent microdeletions in 8q11.2 cause a phenotype suggestive of the 22q11 deletion syndrome.

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Publication year
2010
Author(s)
Ockeloen, C.W.
Leeuw, N. de
Mieloo, H.
Reijnen, I.G.
Vries, L.B.A. de
Source
Clinical Dysmorphology, 19, 3, (2010), pp. 137-9
ISSN
DOI
Annotation
01 juli 2010
Publication type
Article / Letter to editor
Please use this identifier to cite or link to this item: https://hdl.handle.net/2066/87591   https://hdl.handle.net/2066/87591
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