Hotspot for deletions in the CGG repeat region of FMR1 in fragile X patients

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Publication year
1995
Author(s)
Graaff, E. de
Rouillard, P.
Willems, P.J.
Smits, A.P.T.
Rousseau, F.
Oostra, B.A.
Source
Human Molecular Genetics, 4, 1, (1995), pp. 45-49
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Article / Letter to editor
Please use this identifier to cite or link to this item: https://hdl.handle.net/2066/22207   https://hdl.handle.net/2066/22207
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