Vermeesch JR - Search Results

1

Rare copy number variations affecting the synaptic gene DMXL2 in neurodevelopmental disorders.

Costain G, Walker S, Argiropoulos B, Baribeau DA, Bassett AS, Boot E, Devriendt K, Kellam B, Marshall CR, Prasad A, Serrano MA, Stavropoulos DJ, Twede H, Vermeesch JR, Vorstman JAS, Scherer SW. Costain G, et al. Among authors: vermeesch jr. J Neurodev Disord. 2019 Feb 7;11(1):3. doi: 10.1186/s11689-019-9263-3. J Neurodev Disord. 2019. PMID: 30732576 Free PMC article.

2

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. Hum Genet. 1997 Jun;99(6):735-7. doi: 10.1007/s004390050440. Hum Genet. 1997. PMID: 9187665

3

Unusual de novo t(13;15)(q12.1;p13) translocation leading to complex mosaicism including jumping translocation.

Petit P, Devriendt K, Vermeesch JR, De Cock P, Fryns JP. Petit P, et al. Among authors: vermeesch jr. Ann Genet. 1998;41(1):22-6. Ann Genet. 1998. PMID: 9599647

4

Localization by FISH of centric fission breakpoints in a de novo trisomy 9p patient with i(9p) and t(9q;11p).

Petit P, Devriendt K, Vermeesch JR, Meireleire J, Fryns JP. Petit P, et al. Among authors: vermeesch jr. Genet Couns. 1998;9(3):215-21. Genet Couns. 1998. PMID: 9777345

5

Cryptic translocation t(5;18) in familial mental retardation.

Vogels A, Devriendt K, Vermeesch JR, Van Dael R, Marynen P, Dewaele P, Hageman J, Holvoet M, Fryns JP. Vogels A, et al. Among authors: vermeesch jr. Ann Genet. 2000 Jul-Dec;43(3-4):117-23. doi: 10.1016/s0003-3995(00)01024-8. Ann Genet. 2000. PMID: 11164192

6

Ring syndrome caused by ring chromosome 7 without loss of subtelomeric sequences.

Vermeesch JR, Baten E, Fryns JP, Devriendt K. Vermeesch JR, et al. Clin Genet. 2002 Nov;62(5):415-7. doi: 10.1034/j.1399-0004.2002.620511.x. Clin Genet. 2002. PMID: 12431259

7

Partial monosomy 11q and trisomy 12q: variable expression in two siblings.

Lukusa T, Holvoet M, Vermeesch JR, Devriendt K, Fryns JP. Lukusa T, et al. Among authors: vermeesch jr. Genet Couns. 2003;14(2):155-64. Genet Couns. 2003. PMID: 12872809

8

Deletion 2q37.3 and autism: molecular cytogenetic mapping of the candidate region for autistic disorder.

Lukusa T, Vermeesch JR, Holvoet M, Fryns JP, Devriendt K. Lukusa T, et al. Among authors: vermeesch jr. Genet Couns. 2004;15(3):293-301. Genet Couns. 2004. PMID: 15517821

9

Chromosomal phenotypes and submicroscopic abnormalities.

Devriendt K, Vermeesch JR. Devriendt K, et al. Among authors: vermeesch jr. 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.

10

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: vermeesch jr. 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

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