Vermeesch JR - Search Results

1

Array comparative genomic hybridization as a diagnostic tool for syndromic heart defects.

Breckpot J, Thienpont B, Peeters H, de Ravel T, Singer A, Rayyan M, Allegaert K, Vanhole C, Eyskens B, Vermeesch JR, Gewillig M, Devriendt K. Breckpot J, et al. Among authors: vermeesch jr. J Pediatr. 2010 May;156(5):810-7, 817.e1-817.e4. doi: 10.1016/j.jpeds.2009.11.049. Epub 2010 Feb 6. J Pediatr. 2010. PMID: 20138633

2

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. Among authors: vermeesch jr. 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.

3

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

4

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

5

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

6

Delineation of the critical deletion region for congenital heart defects, on chromosome 8p23.1.

Devriendt K, Matthijs G, Van Dael R, Gewillig M, Eyskens B, Hjalgrim H, Dolmer B, McGaughran J, Bröndum-Nielsen K, Marynen P, Fryns JP, Vermeesch JR. Devriendt K, et al. Among authors: vermeesch jr. Am J Hum Genet. 1999 Apr;64(4):1119-26. doi: 10.1086/302330. Am J Hum Genet. 1999. PMID: 10090897 Free PMC article.

7

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

8

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

9

De novo interstitial tandem duplication of chromosome 20p12.1p13.

de Ravel TJ, Vermeesch JR, Fryns JP. de Ravel TJ, et al. Among authors: vermeesch jr. Am J Med Genet A. 2003 Feb 15;117A(1):76-9. doi: 10.1002/ajmg.a.10825. Am J Med Genet A. 2003. PMID: 12548744

10

No evidence for a parental inversion polymorphism predisposing to rearrangements at 22q11.2 in the DiGeorge/Velocardiofacial syndrome.

Gebhardt GS, Devriendt K, Thoelen R, Swillen A, Pijkels E, Fryns JP, Vermeesch JR, Gewillig M. Gebhardt GS, et al. Among authors: vermeesch jr. Eur J Hum Genet. 2003 Feb;11(2):109-11. doi: 10.1038/sj.ejhg.5200930. Eur J Hum Genet. 2003. PMID: 12634857 No abstract available.

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