Wuyts W - Search Results

1

Expanding the spectrum of FOXC1 and PITX2 mutations and copy number changes in patients with anterior segment malformations.

D'haene B, Meire F, Claerhout I, Kroes HY, Plomp A, Arens YH, de Ravel T, Casteels I, De Jaegere S, Hooghe S, Wuyts W, van den Ende J, Roulez F, Veenstra-Knol HE, Oldenburg RA, Giltay J, Verheij JB, de Faber JT, Menten B, De Paepe A, Kestelyn P, Leroy BP, De Baere E. D'haene B, et al. Among authors: wuyts w. Invest Ophthalmol Vis Sci. 2011 Jan 21;52(1):324-33. doi: 10.1167/iovs.10-5309. Invest Ophthalmol Vis Sci. 2011. PMID: 20881294

2

Multiplex ligation-dependent probe amplification to detect subtelomeric rearrangements in routine diagnostics.

Rooms L, Reyniers E, Wuyts W, Storm K, van Luijk R, Scheers S, Wauters J, van den Ende J, Biervliet M, Eyskens F, van Goethem G, Laridon A, Ceulemans B, Courtens W, Kooy RF. Rooms L, et al. Among authors: wuyts w. Clin Genet. 2006 Jan;69(1):58-64. doi: 10.1111/j.1399-0004.2005.00545.x. Clin Genet. 2006. PMID: 16451137

3

Recurrent mutation in the first zinc finger of the orphan nuclear receptor NR2E3 causes autosomal dominant retinitis pigmentosa.

Coppieters F, Leroy BP, Beysen D, Hellemans J, De Bosscher K, Haegeman G, Robberecht K, Wuyts W, Coucke PJ, De Baere E. Coppieters F, et al. Among authors: wuyts w. Am J Hum Genet. 2007 Jul;81(1):147-57. doi: 10.1086/518426. Epub 2007 May 24. Am J Hum Genet. 2007. PMID: 17564971 Free PMC article.

4

Role of Targeted Next Generation Sequencing in the Etiological Work-Up of Congenitally Deaf Children.

Boudewyns A, van den Ende J, Sommen M, Wuyts W, Peeters N, Van de Heyning P, Van Camp G. Boudewyns A, et al. Among authors: wuyts w. Otol Neurotol. 2018 Jul;39(6):732-738. doi: 10.1097/MAO.0000000000001847. Otol Neurotol. 2018. PMID: 29889784

5

[No title available]

[No authors listed] [No authors listed] PMID: 32769956

6

Etiological Work-up in Referrals From Neonatal Hearing Screening: 20 Years of Experience.

Boudewyns A, van den Ende J, Declau F, Wuyts W, Peeters N, Brandt AHD, Van Camp G. Boudewyns A, et al. Among authors: wuyts w. Otol Neurotol. 2020 Oct;41(9):1240-1248. doi: 10.1097/MAO.0000000000002758. Otol Neurotol. 2020. PMID: 32925850

7

Refined physical mapping and genomic structure of the EXTL1 gene.

Wuyts W, Spieker N, Van Roy N, De Boulle K, De Paepe A, Willems PJ, Van Hul W, Versteeg R, Speleman F. Wuyts W, et al. Cytogenet Cell Genet. 1999;86(3-4):267-70. doi: 10.1159/000015317. Cytogenet Cell Genet. 1999. PMID: 10575224

8

Identification of a 52 kb deletion downstream of the SOST gene in patients with van Buchem disease.

Balemans W, Patel N, Ebeling M, Van Hul E, Wuyts W, Lacza C, Dioszegi M, Dikkers FG, Hildering P, Willems PJ, Verheij JB, Lindpaintner K, Vickery B, Foernzler D, Van Hul W. Balemans W, et al. Among authors: wuyts w. J Med Genet. 2002 Feb;39(2):91-7. doi: 10.1136/jmg.39.2.91. J Med Genet. 2002. PMID: 11836356 Free PMC article.

9

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

10

Mutation screening of EXT1 and EXT2 by denaturing high-performance liquid chromatography, direct sequencing analysis, fluorescence in situ hybridization, and a new multiplex ligation-dependent probe amplification probe set in patients with multiple osteochondromas.

Jennes I, Entius MM, Van Hul E, Parra A, Sangiorgi L, Wuyts W. Jennes I, et al. Among authors: wuyts w. J Mol Diagn. 2008 Jan;10(1):85-92. doi: 10.2353/jmoldx.2008.070086. Epub 2007 Dec 28. J Mol Diagn. 2008. PMID: 18165274 Free PMC article.

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