Devriendt K - Search Results

1

Pseudoautosomal region 1 length polymorphism in the human population.

Mensah MA, Hestand MS, Larmuseau MH, Isrie M, Vanderheyden N, Declercq M, Souche EL, Van Houdt J, Stoeva R, Van Esch H, Devriendt K, Voet T, Decorte R, Robinson PN, Vermeesch JR. Mensah MA, et al. Among authors: devriendt k. PLoS Genet. 2014 Nov 6;10(11):e1004578. doi: 10.1371/journal.pgen.1004578. eCollection 2014 Nov. PLoS Genet. 2014. PMID: 25375121 Free PMC article.

2

Chromosomal phenotypes and submicroscopic abnormalities.

Devriendt K, Vermeesch JR. Devriendt K, et al. Hum Genomics. 2004 Jan;1(2):126-33. doi: 10.1186/1479-7364-1-2-126. Hum Genomics. 2004. PMID: 15601540 Free PMC article. Review.

3

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

4

Deletion of VCX-A due to NAHR plays a major role in the occurrence of mental retardation in patients with X-linked ichthyosis.

Van Esch H, Hollanders K, Badisco L, Melotte C, Van Hummelen P, Vermeesch JR, Devriendt K, Fryns JP, Marynen P, Froyen G. Van Esch H, et al. Among authors: devriendt k. Hum Mol Genet. 2005 Jul 1;14(13):1795-803. doi: 10.1093/hmg/ddi186. Epub 2005 May 11. Hum Mol Genet. 2005. PMID: 15888481

5

Anterior cervical hypertrichosis and mental retardation.

Thienpont B, Vermeesch J, Devriendt K. Thienpont B, et al. Among authors: devriendt k. Clin Dysmorphol. 2006 Jul;15(3):189-190. doi: 10.1097/01.mcd.0000204988.39119.9d. Clin Dysmorphol. 2006. PMID: 16760744

6

Identification and characterization of the TRIP8 and REEP3 genes on chromosome 10q21.3 as novel candidate genes for autism.

Castermans D, Vermeesch JR, Fryns JP, Steyaert JG, Van de Ven WJ, Creemers JW, Devriendt K. Castermans D, et al. Among authors: devriendt k. Eur J Hum Genet. 2007 Apr;15(4):422-31. doi: 10.1038/sj.ejhg.5201785. Epub 2007 Feb 7. Eur J Hum Genet. 2007. PMID: 17290275

7

Left-ventricular non-compaction in a patient with monosomy 1p36.

Thienpont B, Mertens L, Buyse G, Vermeesch JR, Devriendt K. Thienpont B, et al. Among authors: devriendt k. Eur J Med Genet. 2007 May-Jun;50(3):233-6. doi: 10.1016/j.ejmg.2007.01.002. Epub 2007 Jan 27. Eur J Med Genet. 2007. PMID: 17337261

8

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.

9

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

10

Subtelomeric imbalances in phenotypically normal individuals.

Balikova I, Menten B, de Ravel T, Le Caignec C, Thienpont B, Urbina M, Doco-Fenzy M, de Rademaeker M, Mortier G, Kooy F, van den Ende J, Devriendt K, Fryns JP, Speleman F, Vermeesch JR. Balikova I, et al. Among authors: devriendt k. Hum Mutat. 2007 Oct;28(10):958-67. doi: 10.1002/humu.20537. Hum Mutat. 2007. PMID: 17492636

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