Willekens D - Search Results

1

Three young children with Smith-Magenis syndrome: their distinct, recognisable behavioural phenotype as the most important clinical symptoms.

Willekens D, De Cock P, Fryns JP. Willekens D, et al. Genet Couns. 2000;11(2):103-10. Genet Couns. 2000. PMID: 10893661

2

Emotional and behavioral profile and child psychiatric diagnosis in the childhood type of myotonic dystrophy.

Goossens E, Steyaert J, De Die-Smulders C, Willekens D, Fryns JP. Goossens E, et al. Among authors: willekens d. Genet Couns. 2000;11(4):317-27. Genet Couns. 2000. PMID: 11140408

3

Terminal 6q25.3 deletion and abnormal behaviour.

Lukusa T, Willekens D, Lukusa N, De Cock F, Fryns JP. Lukusa T, et al. Among authors: willekens d. Genet Couns. 2001;12(3):213-21. Genet Couns. 2001. PMID: 11693783

4

The long term evolution of 6 adult patients with Cohen syndrome and their behavioral characteristics.

Peeters K, Willekens D, Steyaert J, Fryns JP. Peeters K, et al. Among authors: willekens d. Genet Couns. 2008;19(1):1-14. Genet Couns. 2008. PMID: 18564496

5

A study of the cognitive and psychological profile in 16 children with congenital or juvenile myotonic dystrophy.

Steyaert J, Umans S, Willekens D, Legius E, Pijkels E, de Die-Smulders C, Van den Berghe H, Fryns JP. Steyaert J, et al. Among authors: willekens d. Clin Genet. 1997 Sep;52(3):135-41. doi: 10.1111/j.1399-0004.1997.tb02533.x. Clin Genet. 1997. PMID: 9377801

6

Marden-Walker syndrome versus isolated distal arthrogryposis: evidence that both conditions may be variable manifestations of the same mutated gene.

Fryns JP, Willekens D, Van Schoubroeck D, Moerman P. Fryns JP, et al. Among authors: willekens d. Clin Genet. 1998 Jul;54(1):86-9. doi: 10.1111/j.1399-0004.1998.tb03701.x. Clin Genet. 1998. PMID: 9727748

7

Prader-Willi syndrome: new insights in the behavioural and psychiatric spectrum.

Descheemaeker MJ, Vogels A, Govers V, Borghgraef M, Willekens D, Swillen A, Verhoeven W, Fryns JP. Descheemaeker MJ, et al. Among authors: willekens d. J Intellect Disabil Res. 2002 Jan;46(Pt 1):41-50. doi: 10.1046/j.1365-2788.2002.00354.x. J Intellect Disabil Res. 2002. PMID: 11851855

8

Holoprosencephaly and ZIC2 microdeletions: novel clinical and epidemiological specificities delineated.

Chabchoub E, Willekens D, Vermeesch JR, Fryns JP. Chabchoub E, et al. Among authors: willekens d. Clin Genet. 2012 Jun;81(6):584-9. doi: 10.1111/j.1399-0004.2011.01684.x. Epub 2011 May 23. Clin Genet. 2012. PMID: 21496007

9

Re-evaluation of MRX36 family after discovery of an ARX gene mutation reveals mild neurological features of Partington syndrome.

Frints SG, Froyen G, Marynen P, Willekens D, Legius E, Fryns JP. Frints SG, et al. Among authors: willekens d. Am J Med Genet. 2002 Nov 1;112(4):427-8. doi: 10.1002/ajmg.10628. Am J Med Genet. 2002. PMID: 12376949 No abstract available.

10

Behavioral phenotype in childhood type of dystrophia myotonica.

Steyaert J, de Die-Smulders C, Fryns JP, Goossens E, Willekens D. Steyaert J, et al. Among authors: willekens d. Am J Med Genet. 2000 Dec 4;96(6):888-9. doi: 10.1002/1096-8628(20001204)96:6<888::aid-ajmg42>3.0.co;2-7. Am J Med Genet. 2000. PMID: 11121206 No abstract available.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

12 results

Search Page