Zobrazeno 1 - 10
of 1 152
pro vyhledávání: '"Vermeesch Joris"'
Autor:
LeJeune Charlotte, Dierickx Daan, Wildiers Hans, Lannoo Lore, Van Calsteren Kristel, Vandecaveye Vincent, Menten Björn, Vermeesch Joris, Amant Frédéric
Publikováno v:
Gynecologic Oncology Reports, Vol 39, Iss , Pp 100937- (2022)
Background: Breast cancer and hematological cancers are the most commonly diagnosed malignancies during pregnancy. This case report is the first to describe the ultimate challenge to preserve a pregnancy while the expectant mother is diagnosed and tr
Externí odkaz:
https://doaj.org/article/947b21b4a1b9460e84325d8e4105636f
Autor:
Devriendt Koen, Vermeesch Joris R
Publikováno v:
Human Genomics, Vol 1, Iss 2, Pp 126-133 (2004)
Abstract The finding, during the last decade, that several common, clinically delineated syndromes are caused by submicroscopic deletions or, more rarely, by duplications, has provided a powerful tool in the annotation of the human genome. Since most
Externí odkaz:
https://doaj.org/article/106ac45b51c149d78c900c39b6294201
Autor:
Siermann, Maria, Vermeesch, Joris R., Raivio, Taneli, Vanhie, Arne, Peeraer, Karen, Tšuiko, Olga, Borry, Pascal
Publikováno v:
In Reproductive BioMedicine Online September 2024 49(3)
Autor:
Siermann, Maria, Valcke, Ophelia, Vermeesch, Joris Robert, Raivio, Taneli, Tšuiko, Olga, Borry, Pascal
Publikováno v:
In Social Science & Medicine February 2024 343
Autor:
Robberecht Caroline, Voet Thierry, Utine Gülen E, Schinzel Albert, de Leeuw Nicole, Fryns Jean-Pierre, Vermeesch Joris
Publikováno v:
Molecular Cytogenetics, Vol 5, Iss 1, p 19 (2012)
Abstract Structural copy number variation (CNV) is a frequent cause of human variation and disease. Evidence is mounting that somatic acquired CNVs are prevalent, with mosaicisms of large segmental CNVs in blood found in up to one percent of both the
Externí odkaz:
https://doaj.org/article/8f775cedf7b04b3085933d3596b7610f
Autor:
Vermeesch Joris, Andrieux Joris, Desai Manisha, Sheth Jayesh, Weise Anja, Kosyakova Nadezda, Ewers Elisabeth, Sheth Frenny, Hamid Ahmed B, Ziegler Monika, Liehr Thomas
Publikováno v:
Molecular Cytogenetics, Vol 2, Iss 1, p 22 (2009)
Abstract Background Small supernumerary marker chromosomes (sSMC) can be present in numerically abnormal karyotypes like in a 'Turner-syndrome karyotype' mos 45,X/46,X,+mar. Results Here we report the first case of an sSMC found in Turner syndrome ka
Externí odkaz:
https://doaj.org/article/b7686302dc4c4624987736eb9c4b738e
An experimental loop design for the detection of constitutional chromosomal aberrations by array CGH
Autor:
De Moor Bart, Hannes Femke, Van Vooren Steven, Allemeersch Joke, Vermeesch Joris, Moreau Yves
Publikováno v:
BMC Bioinformatics, Vol 10, Iss 1, p 380 (2009)
Abstract Background Comparative genomic hybridization microarrays for the detection of constitutional chromosomal aberrations is the application of microarray technology coming fastest into routine clinical application. Through genotype-phenotype ass
Externí odkaz:
https://doaj.org/article/951d6c56e1a742aea49e55863cedd595
Autor:
Debiec-Rychter Maria, Sciot Raf, Bowers Naomi, Van Calenbergh Frank, Evans Gareth D, de Cock Paul, Brems Hilde, Denayer Ellen, Vermeesch Joris V, Fryns Jean-Pierre, Legius Eric
Publikováno v:
BMC Medical Genetics, Vol 10, Iss 1, p 97 (2009)
Abstract Background Ring chromosome 22 is a rare human constitutional cytogenetic abnormality. Clinical features of neurofibromatosis type 1 and 2 as well as different tumour types have been reported in patients with ring chromosome 22. The pathogene
Externí odkaz:
https://doaj.org/article/6a01ba24aed24e49885d00375788debe
Autor:
Oliveira Guiomar, Kosyakova Nadezda, Weise Anja, Vermeesch Joris, Backx Liesbeth, Rodrigues Carlos, Melo Joana B, Carreira Isabel M, Matoso Eunice
Publikováno v:
Molecular Cytogenetics, Vol 2, Iss 1, p 16 (2009)
Abstract Background Inverted duplications (inv dup) of a terminal chromosome region are a particular subset of rearrangements that often results in partial tetrasomy or partial trisomy when accompanied by a deleted chromosome. Associated mosaicism co
Externí odkaz:
https://doaj.org/article/6a16979014b940469b4f6e06375c7b51
Autor:
Kille Peter, Lavasani Shahin, Cooper Mike, Cai Christine, Richardson Rob, Giesler Theresa, Dar Mubasher, Voet Thierry, Vermeesch Joris
Publikováno v:
BMC Biotechnology, Vol 8, Iss 1, p 86 (2008)
Abstract Background Array-based comparative genomic hybridization (CGH) and gene expression profiling have become vital techniques for identifying molecular defects underlying genetic diseases. Regardless of the microarray platform, cyanine dyes (Cy3
Externí odkaz:
https://doaj.org/article/026ffad9db5d49719727ba302c4a511b