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Results: 1-3 |
Results: 3
PTEN mutation in a family with Cowden syndrome and autism
Authors: Goffin, A Hoefsloot, LH Bosgoed, E Swillen, A Fryns, JP
Citation: A. Goffin et al., PTEN mutation in a family with Cowden syndrome and autism, AM J MED G, 105(6), 2001, pp. 521-524
Chromosome 22q11 deletion syndrome: Update and review of the clinical features, cognitive-behavioral spectrum, and psychiatric complications
Authors: Swillen, A Vogels, A Devriendt, K Fryns, JP
Citation: A. Swillen et al., Chromosome 22q11 deletion syndrome: Update and review of the clinical features, cognitive-behavioral spectrum, and psychiatric complications, AM J MED G, 97(2), 2000, pp. 128-135
Familial deletions of chromosome 22q11: The Leuven experience
Authors: Swillen, A Devriendt, K Vantrappen, G Vogels, A Rommel, N Fryns, JP Eyskens, B Gewillig, M Dumoulin, M
Citation: A. Swillen et al., Familial deletions of chromosome 22q11: The Leuven experience, AM J MED G, 80(5), 1998, pp. 531-532
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