Wuyts W - Search Results

1

Clinical, cytogenetic, and molecular characterization of a patient with a de novo interstitial 22q12 duplication.

Gentile M, Wuyts W, Grittani S, Di Carlo A, Cariola F, Verdyck P, Margari L, Perniola T, Buonadonna AL. Gentile M, et al. Among authors: wuyts w. Am J Med Genet A. 2004 Jun 1;127A(2):186-90. doi: 10.1002/ajmg.a.20672. Am J Med Genet A. 2004. PMID: 15108208

2

A novel mutation in the MSX2 gene in a family with foramina parietalia permagna (FPP).

Spruijt L, Verdyck P, Van Hul W, Wuyts W, de Die-Smulders C. Spruijt L, et al. Among authors: wuyts w. Am J Med Genet A. 2005 Nov 15;139(1):45-7. doi: 10.1002/ajmg.a.30923. Am J Med Genet A. 2005. PMID: 16222674 No abstract available.

3

Clinical and molecular analysis of nine families with Adams-Oliver syndrome.

Verdyck P, Holder-Espinasse M, Hul WV, Wuyts W. Verdyck P, et al. Among authors: wuyts w. Eur J Hum Genet. 2003 Jun;11(6):457-63. doi: 10.1038/sj.ejhg.5200980. Eur J Hum Genet. 2003. PMID: 12774039

4

Adams-Oliver syndrome: clinical description of a four-generation family and exclusion of five candidate genes.

Verdyck P, Blaumeiser B, Holder-Espinasse M, Van Hul W, Wuyts W. Verdyck P, et al. Among authors: wuyts w. Clin Genet. 2006 Jan;69(1):86-92. doi: 10.1111/j.1399-0004.2006.00552.x. Clin Genet. 2006. PMID: 16451141

5

Genetic defects in the development of the skull vault in humans and mice.

Verdyck P, Wuyts W, Van Hul W. Verdyck P, et al. Among authors: wuyts w. Crit Rev Eukaryot Gene Expr. 2006;16(2):119-42. doi: 10.1615/critreveukargeneexpr.v16.i2.20. Crit Rev Eukaryot Gene Expr. 2006. PMID: 16749893 Review.

6

Multiple exostoses, mental retardation, hypertrichosis, and brain abnormalities in a boy with a de novo 8q24 submicroscopic interstitial deletion.

Wuyts W, Roland D, Lüdecke HJ, Wauters J, Foulon M, Van Hul W, Van Maldergem L. Wuyts W, et al. Am J Med Genet. 2002 Dec 15;113(4):326-32. doi: 10.1002/ajmg.10845. Am J Med Genet. 2002. PMID: 12457403

7

A subterminal deletion of the long arm of chromosome 10: a clinical report and review.

Courtens W, Wuyts W, Rooms L, Pera SB, Wauters J. Courtens W, et al. Among authors: wuyts w. Am J Med Genet A. 2006 Feb 15;140(4):402-9. doi: 10.1002/ajmg.a.31053. Am J Med Genet A. 2006. PMID: 16419133

8

Hypoparathyroidism-retardation-dysmorphism syndrome in a girl: A new variant not caused by a TBCE mutation--clinical report and review.

Courtens W, Wuyts W, Poot M, Szuhai K, Wauters J, Reyniers E, Eleveld M, Diaz G, Nöthen MM, Parvari R. Courtens W, et al. Among authors: wuyts w. Am J Med Genet A. 2006 Mar 15;140(6):611-7. doi: 10.1002/ajmg.a.31122. Am J Med Genet A. 2006. PMID: 16470743 Review.

9

An interstitial deletion of chromosome 7 at band q21: a case report and review.

Courtens W, Vermeulen S, Wuyts W, Messiaen L, Wauters J, Nuytinck L, Peeters N, Storm K, Speleman F, Nöthen MM. Courtens W, et al. Among authors: wuyts w. Am J Med Genet A. 2005 Apr 1;134A(1):12-23. doi: 10.1002/ajmg.a.30106. Am J Med Genet A. 2005. PMID: 15732063 Review.

10

Delineation of a contiguous gene syndrome with multiple exostoses, enlarged parietal foramina, craniofacial dysostosis, and mental retardation, caused by deletions in the short arm of chromosome 11.

Bartsch O, Wuyts W, Van Hul W, Hecht JT, Meinecke P, Hogue D, Werner W, Zabel B, Hinkel GK, Powell CM, Shaffer LG, Willems PJ. Bartsch O, et al. Among authors: wuyts w. Am J Hum Genet. 1996 Apr;58(4):734-42. Am J Hum Genet. 1996. PMID: 8644736 Free PMC article.

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