Interstitial 6q deletion with a Prader-Willi-like phenotype: a new case and review of the literature.

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Publication year
2000
Author(s)
Gilhuis, H.J.
Ravenswaaij-Arts, C.M.A. van
Hamel, B.C.J.
Gabreëls, F.J.M.
Source
European Journal of Paediatric Neurology, 4, (2000), pp. 39-43
ISSN
Publication type
Article / Letter to editor
Please use this identifier to cite or link to this item:http://hdl.handle.net/2066/150675   http://hdl.handle.net/2066/150675
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