Infant with MCA and severe cutis laxa due to a de novo duplication 11p of paternal origin.

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Publication year
2012
Author(s)
Gardeitchik, T.
Leeuw, N. de
Nijtmans, L.G.J.
Jira, P.
Kozicz, L.T.
Czako, M.
Burgt, C.J.A.M. van der
Morava, E.
Source
American Journal of Medical Genetics. Part A, 158A, 2, (2012), pp. 469-72
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DOI
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01 februari 2012
Publication type
Article / Letter to editor
Please use this identifier to cite or link to this item: https://hdl.handle.net/2066/108339   https://hdl.handle.net/2066/108339
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