M J Eleveld
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Explore the profile of M J Eleveld including associated specialties, affiliations and a list of published articles.
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Articles
9
Citations
104
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Recent Articles
1.
Hochstenbach R, van Gijn M, Krijtenburg P, Raemakers R, van t Slot R, Renkens I, et al.
Mol Syndromol
. 2013 Apr;
3(6):274-83.
PMID: 23599698
In a 24-year-old man with mild intellectual disability, congenital heart defects and obesity, we identified up to 4 small supernumerary marker chromosomes (sSMCs) in blood metaphases. The ring-shaped sSMCs were...
2.
Molzen T, Burghout P, Bootsma H, Brandt C, van der Gaast-de Jongh C, Eleveld M, et al.
Infect Immun
. 2010 Nov;
79(1):288-97.
PMID: 21041497
Meningitis is the most serious of invasive infections caused by the Gram-positive bacterium Streptococcus pneumoniae. Vaccines protect only against a limited number of serotypes, and evolving bacterial resistance to antimicrobials...
3.
Ozgen H, van Daalen E, Bolton P, Maloney V, Huang S, Cresswell L, et al.
Clin Genet
. 2009 Oct;
76(4):348-56.
PMID: 19793310
Autism spectrum disorder (ASD) represents a set of neurodevelopmental disorders with a strong genetic aetiology. Chromosomal rearrangements have been detected in 5-10% of the patients with ASD, and recent applications...
4.
de Pater J, Poot M, Beemer F, Bijlsma J, Hack W, Van Dam W, et al.
Eur J Med Genet
. 2006 Feb;
49(1):19-27.
PMID: 16473306
A female infant with dysmorphic facial features, psychomotor retardation, and clitoris hypertrophy is described. Molecular cytogenetic analyses revealed a de novo unbalanced translocation, causing partial monosomy 1p36 and partial trisomy...
5.
de Pater J, Nikkels P, Poot M, Eleveld M, Stigter R, van der Sijs-Bos C, et al.
Pediatr Dev Pathol
. 2005 Oct;
8(4):497-503.
PMID: 16222479
During routine ultrasound screening at 12 weeks 5 days of gestation, a nuchal translucency of 7 mm, an omphalocele, and fetal hydrops were found and prompted chorionic villus sampling at...
6.
Lichtenbelt K, Hochstenbach R, Van Dam W, Eleveld M, Poot M, Beemer F
Am J Med Genet A
. 2004 Dec;
132A(1):93-100.
PMID: 15580634
We report a girl with severe retardation of expressive speech development carrying a small, supernumerary ring chromosome derived from the proximal region of the long arm of chromosome 7. The...
7.
Eleveld M, Bodmer D, Merkx G, Siepman A, Sprenger S, Weterman M, et al.
Genes Chromosomes Cancer
. 2001 Apr;
31(1):23-32.
PMID: 11284032
We identified a novel familial case of clear-cell renal cancer and a t(3;6)(q12;q15). Subsequent cytogenetic and molecular analyses showed the presence of several abnormalities within tumour samples obtained from different...
8.
Simons A, Jeuken J, Eleveld M, Boerman R, Geurts van Kessel A
J Pathol
. 1999 Nov;
189(3):402-9.
PMID: 10547603
Representational difference analysis (RDA) of a human glioblastoma xenograft resulted in the isolation of five tumour-associated homozygously deleted DNA fragments, all originating from chromosome 9, region p21. Subsequent analysis of...
9.
Bodmer D, Eleveld M, Ligtenberg M, Weterman M, Janssen B, Smeets D, et al.
Am J Hum Genet
. 1998 Jun;
62(6):1475-83.
PMID: 9585616
Through allele-segregation and loss-of-heterozygosity analyses, we demonstrated loss of the translocation-derivative chromosome 3 in five independent renal cell tumors of the clear-cell type, obtained from three members of a family...