Vermeesch JR - Search Results

1

Tetrasomy 12pter-12p13.31 in a girl with partial Pallister-Killian syndrome phenotype.

Vermeesch JR, Melotte C, Salden I, Riegel M, Trifnov V, Polityko A, Rumyantseva N, Naumchik I, Starke H, Matthijs G, Schinzel A, Fryns JP, Liehr T. Vermeesch JR, et al. Eur J Med Genet. 2005 Jul-Sep;48(3):319-27. doi: 10.1016/j.ejmg.2005.04.018. Eur J Med Genet. 2005. PMID: 16179227

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

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

6

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

7

Noonan-like phenotype in monozygotic twins with a duplication-deficiency of the long arm of chromosome 18 resulting from a maternal paracentric inversion.

Courtens W, Grossman D, Van Roy N, Messiaen L, Vamos E, Toppet V, Haumont D, Streydio C, Jauch A, Vermeesch JR, Speleman F. Courtens W, et al. Among authors: vermeesch jr. Hum Genet. 1998 Oct;103(4):497-505. doi: 10.1007/s004390050857. Hum Genet. 1998. PMID: 9856497

8

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.

9

A mosaic extra ring chromosome 4 in a female patient with postnatal overgrowth.

Vermeesch JR, Petit P, Dutra A, Schröck E, Ried T, Fryns JP. Vermeesch JR, et al. Genet Couns. 1999;10(2):195-6. Genet Couns. 1999. PMID: 10422016 No abstract available.

10

Multiple small accessory marker chromosomes from different centromeric origin in a moderately mentally retarded male.

Vermeesch JR, Duhamel H, Petit P, Falzetti D, Fryns JP, Marynen P. Vermeesch JR, et al. Hum Genet. 1999 Dec;105(6):611-8. doi: 10.1007/s004399900184. Hum Genet. 1999. PMID: 10647897

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