Devriendt K - Search Results

1

Diagnostic evaluation for asymmetry: consider genetic mosaicism.

Devriendt K, Fryns JP. Devriendt K, et al. Eur J Pediatr. 2004 Oct;163(10):634-5. doi: 10.1007/s00431-004-1499-5. Eur J Pediatr. 2004. PMID: 15290260 No abstract available.

2

Velocardiofacial syndrome presenting as distal arthrogryposis.

Devriendt K, Swillen A, Gewillig M, Fryns JP, Moens P, De Smet L. Devriendt K, et al. Eur J Pediatr. 2004 Jun;163(6):329-30. doi: 10.1007/s00431-004-1429-6. Eur J Pediatr. 2004. PMID: 15346917 No abstract available.

3

What's new in karyotyping? The move towards array comparative genomic hybridisation (CGH).

de Ravel TJ, Devriendt K, Fryns JP, Vermeesch JR. de Ravel TJ, et al. Among authors: devriendt k. Eur J Pediatr. 2007 Jul;166(7):637-43. doi: 10.1007/s00431-007-0463-6. Epub 2007 Mar 20. Eur J Pediatr. 2007. PMID: 17372759 Free article. Review.

4

Submicroscopic chromosomal imbalances detected by array-CGH are a frequent cause of congenital heart defects in selected patients.

Thienpont B, Mertens L, de Ravel T, Eyskens B, Boshoff D, Maas N, Fryns JP, Gewillig M, Vermeesch JR, Devriendt K. Thienpont B, et al. Among authors: devriendt k. Eur Heart J. 2007 Nov;28(22):2778-84. doi: 10.1093/eurheartj/ehl560. Epub 2007 Mar 23. Eur Heart J. 2007. PMID: 17384091

5

Somatic mosaicism and variable expression of Townes-Brocks syndrome.

Devriendt K, Fryns JP, Lemmens F, Kohlhase J, Liebers M. Devriendt K, et al. Am J Med Genet. 2002 Aug 1;111(2):230-1. doi: 10.1002/ajmg.10485. Am J Med Genet. 2002. PMID: 12210359 No abstract available.

6

Multiple circumferential skin creases: another sign of genetic mosaicism?

Devriendt K, Fryns JP, Vanhole C, Bogaert G. Devriendt K, et al. Am J Med Genet A. 2004 Dec 1;131(2):219-20. doi: 10.1002/ajmg.a.30324. Am J Med Genet A. 2004. PMID: 15384095 No abstract available.

7

Iris heterochromia: a variable feature in Verloes-Koulischer-oral-acral syndrome.

Mathijssen IB, Fryns JP, Devriendt K, Sznajer Y, Van Eygen M. Mathijssen IB, et al. Among authors: devriendt k. Am J Med Genet A. 2005 Jan 30;132A(3):338-9. doi: 10.1002/ajmg.a.30427. Am J Med Genet A. 2005. PMID: 15578617 No abstract available.

8

Glypican 1 gene: good candidate for brachydactyly type E.

Syrrou M, Keymolen K, Devriendt K, Holvoet M, Thoelen R, Verhofstadt K, Fryns JP. Syrrou M, et al. Among authors: devriendt k. Am J Med Genet. 2002 Apr 1;108(4):310-4. doi: 10.1002/ajmg.10266. Am J Med Genet. 2002. PMID: 11920836

9

Molecular karyotyping: array CGH quality criteria for constitutional genetic diagnosis.

Vermeesch JR, Melotte C, Froyen G, Van Vooren S, Dutta B, Maas N, Vermeulen S, Menten B, Speleman F, De Moor B, Van Hummelen P, Marynen P, Fryns JP, Devriendt K. Vermeesch JR, et al. Among authors: devriendt k. J Histochem Cytochem. 2005 Mar;53(3):413-22. doi: 10.1369/jhc.4A6436.2005. J Histochem Cytochem. 2005. PMID: 15750031

10

2q31.1 microdeletion syndrome: redefining the associated clinical phenotype.

Dimitrov B, Balikova I, de Ravel T, Van Esch H, De Smedt M, Baten E, Vermeesch JR, Bradinova I, Simeonov E, Devriendt K, Fryns JP, Debeer P. Dimitrov B, et al. Among authors: devriendt k. J Med Genet. 2011 Feb;48(2):98-104. doi: 10.1136/jmg.2010.079491. Epub 2010 Nov 10. J Med Genet. 2011. PMID: 21068127

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