A boy with a submicroscopic 22qter deletion, general overgrowth and features suggestive of FG syndrome

Author:

De Vries Bba,Bitner-Glindzicz M,Knight Sjl,Tyson J,MacDermot Kd,Flint J,Malcolm S,Winter Rm

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference25 articles.

1. Fragile X syndrome [Review];Wiebe;Can Fam Physician,1994

2. FG syndrome;Thompson;J Med Genet,1987

3. FG syndrome: the triad mental retardation, hypotonia, and constipation reviewed;Zwamborn-Hanssen;Genet Couns,1995

4. A gene for FG syndrome maps in the Xq12-q21.31 region;Briault;Am J Med Genet,1997

5. Fragile X mutation and FG syndrome-like phenotype;Piussan;Am J Med Genet,1996

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