Telomere processing in EuplotesVERMEESCH, J. R; WILLIAMS, D; PRICE, C. M et al.Nucleic acids research. 1993, Vol 21, Num 23, pp 5366-5371, issn 0305-1048Article

A familial complex chromosome translocation resulting in duplication of 6p25VERMEESCH, J. R; THOELEN, R; FRYNS, Jean Pierre et al.Annales de génétique (Paris). 2004, Vol 47, Num 3, pp 275-280, issn 0003-3995, 6 p.Article

Telomeric DNA sequence and structure following de novo telomere synthesis in Euplotes crassusVERMEESCH, J. R; PRICE, C. M.Molecular and cellular biology (Print). 1994, Vol 14, Num 1, pp 554-566, issn 0270-7306Article

De novo interstitial tandem duplication of chromosome 20p12.1p13DE RAVEL, T. J. L; VERMEESCH, J. R; FRYNS, J.-P et al.American journal of medical genetics. 2003, Vol 117A, Num 1, pp 76-79, issn 0148-7299, 4 p.Article

Noonan-like phenotype in monozygotic twins with a duplication-deficiency of the long arm of chromosome 18 resulting from a maternal paracentric inversionCOURTENS, W; GROSSMAN, D; SPELEMAN, F et al.Human genetics. 1998, Vol 103, Num 4, pp 497-505, issn 0340-6717Article

Trisomy 15 rescue with jumping translocation of distal 15q in Prader-Willi syndromeDEVRIENDT, K; PETIT, P; MATTHIJS, G et al.Journal of medical genetics. 1997, Vol 34, Num 5, pp 395-399, issn 0022-2593Article

Assignment of the human glypican gene (GPC1) to 2q35-q37 by fluorescence in situ hybridizationVERMEESCH, J. R; MERTENS, G; DAVID, G et al.Genomics (San Diego, Calif.). 1995, Vol 25, Num 1, pp 327-329, issn 0888-7543Article

Accumulation of telomerase RNA and telomere protein transcripts during telomere synthesis of EuplotesPRICE, C. M; ADAMS, A. K; VERMEESCH, J. R et al.The Journal of eukaryotic microbiology. 1994, Vol 41, Num 3, pp 267-275, issn 1066-5234Article

Holoprosencephaly and ZIC2 microdeletions: novel clinical and epidemiological specificities delineatedCHABCHOUB, E; WILLEKENS, D; VERMEESCH, J. R et al.Clinical genetics. 2012, Vol 81, Num 6, pp 584-589, issn 0009-9163, 6 p.Article

PGD for a complex chromosomal rearrangement by array comparative genomic hybridizationVANNESTE, E; MELOTTE, C; VERMEESCH, J. R et al.Human reproduction (Oxford. Print). 2011, Vol 26, Num 4, pp 941-949, issn 0268-1161, 9 p.Article

Recurrent reciprocal deletions and duplications of 16p13.11 : the deletion is a risk factor for MR/MCA while the duplication may be a rare benign variantHANNES, F. D; SHARP, A. J; STEWART, H et al.Journal of medical genetics. 2009, Vol 46, Num 4, pp 223-232, issn 0022-2593, 10 p.Article

Mild Wolf-Hirschhorn syndrome: micro-array CGH analysis of atypical 4p16.3 deletions enables refinement of the genotype-phenotype mapVAN BUGGENHOUT, G; MELOTTE, C; VERMEESCH, J. R et al.Journal of medical genetics. 2004, Vol 41, Num 9, pp 691-698, issn 0022-2593, 8 p.Article

Multiple small accessory marker chromosomes from different centromeric origin in a moderately mentally retarded maleVERMEESCH, J. R; DUHAMEL, H; PETIT, P et al.Human genetics. 1999, Vol 105, Num 6, pp 611-618, issn 0340-6717Article

Further delineation of the 15q13 microdeletion and duplication syndromes: a clinical spectrum varying from non-pathogenic to a severe outcomeVAN BON, B. W. M; MEFFORD, H. C; STEWART, H et al.Journal of medical genetics. 2009, Vol 46, Num 8, pp 511-523, issn 0022-2593, 13 p.Article

Genotype-phenotype correlation in 21 patients with Wolf-Hirschhorn syndrome using high resolution array comparative genome hybridisation (CGH)MAAS, N. M. C; VAN BUGGENHOUT, G; HORDIJK, R et al.Journal of medical genetics. 2008, Vol 45, Num 2, pp 71-80, issn 0022-2593, 10 p.Article

Chromosome healing of constitutional chromosome deletions studied by microdissectionVERMEESCH, J. R; FALZETTI, D; VAN BUGGENHOUT, G et al.Cytogenetics and cell genetics. 1998, Vol 81, Num 1, pp 68-72, issn 0301-0171Article

Unusual de novo t(13;15)(q12,1;p13) translocation leading to complex mosaicism including jumping translocationPETIT, P; DEVRIENDT, K; VERMEESCH, J. R et al.Annales de génétique (Paris). 1998, Vol 41, Num 1, pp 22-26, issn 0003-3995Article

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, J. R et al.Genetic counseling. 1998, Vol 9, Num 3, pp 215-221, issn 1015-8146Conference Paper

The IL-9 receptor gene, located in the Xq/Yq pseudoautosomal region, has an autosomal origin, escapes X inactivation and is expressed from the YVERMEESCH, J. R; PETIT, P; KERMOUNI, A et al.Human molecular genetics (Print). 1997, Vol 6, Num 1, pp 1-8, issn 0964-6906Article

Oculocerebral Hypopigmentation Syndrome Maps to Chromosome 3q27.1q29CHABCHOUB, E; COGULU, O; DURMAZ, B et al.Dermatology (Basel). 2011, Vol 223, Num 4, pp 306-310, issn 1018-8665, 5 p.Article

Preimplantation genetic diagnosis using fluorescent in situ hybridization for cancer predisposition syndromes caused by microdeletionsVANNESTE, E; MELOTTE, C; DEBROCK, S et al.Human reproduction (Oxford. Print). 2009, Vol 24, Num 6, pp 1522-1528, issn 0268-1161, 7 p.Article

From chromosomes to molecular karyotyping : The del(2)(q32.2q33) deletion syndrome defined by clinical and molecular characterization of four patientsVAN BUGGENHOUT, G; VAN RAVENSWAAIJ-ARTS, C; MAAS, N. M. C et al.European journal of medical genetics. 2005, Vol 48, Num 3, pp 276-289, issn 1769-7212, 14 p.Article

Preimplantation genetic diagnosis for an insertional translocation carrierMELOTTE, C; DEBROCK, S; D'HOOGHE, T et al.Human reproduction (Oxford. Print). 2004, Vol 19, Num 12, pp 2777-2783, issn 0268-1161, 7 p.Article

Microdissection and FISH investigations in acute myeloid leukemia : A step forward to full identification of complex karyotypic changesFALZETTI, D; VERMEESCH, J. R; MATTEUCCI, C et al.Cancer genetics and cytogenetics. 2000, Vol 118, Num 1, pp 28-34, issn 0165-4608Article

Identification of multiple copies of a 20q-chromosome in a case of myelodysplastic syndrome : a FISH studyFALZETTI, D; VERMEESCH, J. R; HOOD, T. L et al.Leukemia research. 1999, Vol 23, Num 4, pp 407-413, issn 0145-2126Article