Pieter Verdyck
Overview
Explore the profile of Pieter Verdyck including associated specialties, affiliations and a list of published articles.
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Snapshot
Articles
13
Citations
119
Followers
0
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Recent Articles
11.
Verdyck P, Berckmoes V, De Vos A, Verpoest W, Liebaers I, Bonduelle M, et al.
Am J Med Genet A
. 2015 May;
167A(10):2306-13.
PMID: 25953684
Fragile X syndrome (FXS), the most common inherited intellectual disability syndrome, is caused by expansion and hypermethylation of the CGG repeat in the 5' UTR of the FMR1 gene. This...
12.
Derks-Smeets I, de Die-Smulders C, Mackens S, van Golde R, Paulussen A, Dreesen J, et al.
Breast Cancer Res Treat
. 2014 Apr;
145(3):673-81.
PMID: 24748567
Preimplantation genetic diagnosis (PGD) is a reproductive option for BRCA1/2 mutation carriers wishing to avoid transmission of the predisposition for hereditary breast and ovarian cancer (HBOC) to their offspring. Embryos...
13.
Verdyck P, Wuyts W, Van Hul W
Crit Rev Eukaryot Gene Expr
. 2006 Jun;
16(2):119-42.
PMID: 16749893
Using a genetic approach, an increasing number of genes has been shown to be important for proper skull vault development. In this review, we discuss the genes involved in disorders...
14.
Spruijt L, Verdyck P, Van Hul W, Wuyts W, de Die-Smulders C
Am J Med Genet A
. 2005 Oct;
139(1):45-7.
PMID: 16222674
No abstract available.
15.
Verdyck P, Holder-Espinasse M, Van Hul W, Wuyts W
Eur J Hum Genet
. 2003 May;
11(6):457-63.
PMID: 12774039
Adams-Oliver syndrome (AOS) is defined by the combination of limb abnormalities and scalp defects, often accompanied by skull ossification defects. We studied nine families affected with AOS, eight of which...