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

Publication year

2000

Author(s)

Ravenswaaij-Arts, C.M.A. van

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: https://hdl.handle.net/2066/150675

https://hdl.handle.net/2066/150675

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