Devriendt K - Search Results

1

Challenges of interpreting copy number variation in syndromic and non-syndromic congenital heart defects.

Breckpot J, Thienpont B, Arens Y, Tranchevent LC, Vermeesch JR, Moreau Y, Gewillig M, Devriendt K. Breckpot J, et al. Among authors: devriendt k. Cytogenet Genome Res. 2011;135(3-4):251-9. doi: 10.1159/000331272. Epub 2011 Sep 13. Cytogenet Genome Res. 2011. PMID: 21921585 Review.

2

Asplenia syndrome and isolated total anomalous pulmonary venous connection in siblings.

Devriendt K, Casaer A, Van Cauter A, de Zegher F, Dumoulin M, Gewillig M, Devlieger H. Devriendt K, et al. Eur J Pediatr. 1994 Oct;153(10):712-4. doi: 10.1007/BF01954484. Eur J Pediatr. 1994. PMID: 7813525

3

Terminal deletion in chromosome region 8p23.1-8pter in a child with features of velo-cardio-facial syndrome.

Devriendt K, De Mars K, De Cock P, Gewillig M, Fryns JP. Devriendt K, et al. Ann Genet. 1995;38(4):228-30. Ann Genet. 1995. PMID: 8629811

4

Renal and urological tract malformations caused by a 22q11 deletion.

Devriendt K, Swillen A, Fryns JP, Proesmans W, Gewillig M. Devriendt K, et al. J Med Genet. 1996 Apr;33(4):349. doi: 10.1136/jmg.33.4.349. J Med Genet. 1996. PMID: 8730297 Free PMC article. No abstract available.

5

The incidence of a deletion in chromosome 22Q11 in sporadic and familial conotruncal heart disease.

Devriendt K, Eyskens B, Swillen A, Dumoulin M, Gewillig M, Fryns JP. Devriendt K, et al. Eur J Pediatr. 1996 Aug;155(8):721. doi: 10.1007/BF01957162. Eur J Pediatr. 1996. PMID: 8839734 No abstract available.

6

Agenesis of corpus callosum and anophthalmia in the asplenia syndrome. A recognisable association?

Devriendt K, Naulaers G, Matthijs G, Van Houdt K, Devlieger H, Gewillig M, Fryns JP. Devriendt K, et al. Ann Genet. 1997;40(1):14-7. Ann Genet. 1997. PMID: 9150845

7

Trisomy 15 rescue with jumping translocation of distal 15q in Prader-Willi syndrome.

Devriendt K, Petit P, Matthijs G, Vermeesch JR, Holvoet M, De Muelenaere A, Marynen P, Cassiman JJ, Fryns JP. Devriendt K, et al. J Med Genet. 1997 May;34(5):395-9. doi: 10.1136/jmg.34.5.395. J Med Genet. 1997. PMID: 9152837 Free PMC article.

8

Submicroscopic deletion in chromosome 22q11 in trizygous triplet siblings and their father. Clinical variability of 22q11 deletion.

Devriendt K, Van Hoestenberghe R, Van Hole C, Devlieger H, Gewillig M, Moerman P, Van den Berghe H, Fryns JP. Devriendt K, et al. Clin Genet. 1997 Apr;51(4):246-9. doi: 10.1111/j.1399-0004.1997.tb02463.x. Clin Genet. 1997. PMID: 9184246

9

Interstitial telomeric sequences at the junction site of a jumping translocation.

Vermeesch JR, Petit P, Speleman F, Devriendt K, Fryns JP, Marynen P. Vermeesch JR, et al. Among authors: devriendt k. Hum Genet. 1997 Jun;99(6):735-7. doi: 10.1007/s004390050440. Hum Genet. 1997. PMID: 9187665

10

Intelligence and psychosocial adjustment in velocardiofacial syndrome: a study of 37 children and adolescents with VCFS.

Swillen A, Devriendt K, Legius E, Eyskens B, Dumoulin M, Gewillig M, Fryns JP. Swillen A, et al. Among authors: devriendt k. J Med Genet. 1997 Jun;34(6):453-8. doi: 10.1136/jmg.34.6.453. J Med Genet. 1997. PMID: 9192263 Free PMC article.

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 Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

606 results

Search Page

Filters