Partial iris hypoplasia in a patient with an interstitial subtelomeric 6p deletion not including the forkhead transcription factor gene FOXC1.

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Publication year
2005
Author(s)
Koolen, D.A.
Knoers, N.V.A.M.
Nillesen, W.M.
Slabbers, G.H.
Smeets, D.F.C.M.
Leeuw, N. de
Sistermans, E.A.
Vries, L.B.A. de
Source
European Journal of Human Genetics, 13, 11, (2005), pp. 1169-71
ISSN
DOI
Publication type
Article / Letter to editor
Please use this identifier to cite or link to this item: https://hdl.handle.net/2066/47530   https://hdl.handle.net/2066/47530
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