Vermeesch JR - Search Results

1

Emerging patterns of cryptic chromosomal imbalance in patients with idiopathic mental retardation and multiple congenital anomalies: a new series of 140 patients and review of published reports.

Menten B, Maas N, Thienpont B, Buysse K, Vandesompele J, Melotte C, de Ravel T, Van Vooren S, Balikova I, Backx L, Janssens S, De Paepe A, De Moor B, Moreau Y, Marynen P, Fryns JP, Mortier G, Devriendt K, Speleman F, Vermeesch JR. Menten B, et al. Among authors: vermeesch jr. J Med Genet. 2006 Aug;43(8):625-33. doi: 10.1136/jmg.2005.039453. Epub 2006 Feb 20. J Med Genet. 2006. PMID: 16490798 Free PMC article.

2

A physical map of the region spanning the chromosome 12 translocation breakpoint in a mesothelioma with a t(X;12)(q22;p13).

Aerssens J, Guo C, Vermeesch J, Baens M, Browne D, Litt M, Van Den Berghe H, Marynen P. Aerssens J, et al. Cytogenet Cell Genet. 1995;71(3):268-75. doi: 10.1159/000134125. Cytogenet Cell Genet. 1995. PMID: 7587392

3

Assignment of the human glypican gene (GPC1) to 2q35-q37 by fluorescence in situ hybridization.

Vermeesch JR, Mertens G, David G, Marynen P. Vermeesch JR, et al. Genomics. 1995 Jan 1;25(1):327-9. doi: 10.1016/0888-7543(95)80152-c. Genomics. 1995. PMID: 7774946 No abstract available.

4

Differences in the distribution and nature of the interstitial telomeric (TTAGGG)n sequences in the chromosomes of the Giraffidae, okapai (Okapia johnstoni), and giraffe (Giraffa camelopardalis): evidence for ancestral telomeres at the okapi polymorphic rob(5;26) fusion site.

Vermeesch JR, De Meurichy W, Van Den Berghe H, Marynen P, Petit P. Vermeesch JR, et al. Cytogenet Cell Genet. 1996;72(4):310-5. doi: 10.1159/000134211. Cytogenet Cell Genet. 1996. PMID: 8641137

5

The IL-9 receptor gene, located in the Xq/Yq pseudoautosomal region, has an autosomal origin, escapes X inactivation and is expressed from the Y.

Vermeesch JR, Petit P, Kermouni A, Renauld JC, Van Den Berghe H, Marynen P. Vermeesch JR, et al. Hum Mol Genet. 1997 Jan;6(1):1-8. doi: 10.1093/hmg/6.1.1. Hum Mol Genet. 1997. PMID: 9002663

6

Characterization of glypican-5 and chromosomal localization of human GPC5, a new member of the glypican gene family.

Veugelers M, Vermeesch J, Reekmans G, Steinfeld R, Marynen P, David G. Veugelers M, et al. Genomics. 1997 Feb 15;40(1):24-30. doi: 10.1006/geno.1996.4518. Genomics. 1997. PMID: 9070915

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. 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.

8

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

9

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

10

Chromosome healing of constitutional chromosome deletions studied by microdissection.

Vermeesch JR, Falzetti D, Van Buggenhout G, Fryns JP, Marynen P. Vermeesch JR, et al. Cytogenet Cell Genet. 1998;81(1):68-72. doi: 10.1159/000014991. Cytogenet Cell Genet. 1998. PMID: 9691179

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