Progression from colorectal adenoma to carcinoma is associated with non-random chromosomal gains as detected by comparative genomic hybridisation.

GA Meijer, MA Hermsen, JP Baak… - Journal of clinical …, 1998 - jcp.bmj.com
AIMS: Chromosomal gains and losses were surveyed by comparative genomic hybridisation
(CGH) in a series of colorectal adenomas and carcinomas, in search of high risk genomic …

Common missense mutation G1528C in long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency. Characterization and expression of the mutant protein, mutation …

L IJlst, JP Ruiter, JM Hoovers… - The Journal of …, 1996 - Am Soc Clin Investig
Mitochondrial trifunctional protein (MTP) is a recently identified enzyme involved in
mitochondrial beta-oxidation, harboring long-chain enoyl-CoA hydratase, long-chain 3 …

Expression cloning and chromosomal mapping of the leukocyte activation antigen CD97, a new seven-span transmembrane molecule of the secretion receptor …

J Hamann, W Eichler, D Hamann… - … (Baltimore, Md.: 1950 …, 1995 - journals.aai.org
CD97 is a monomeric glycoprotein of 75 to 85 kDa that is induced rapidly on the surface of
most leukocytes upon activation. We herein report the isolation of a cDNA encoding human …

Multiple genetic loci within 11p15 defined by Beckwith-Wiedemann syndrome rearrangement breakpoints and subchromosomal transferable fragments.

JM Hoovers, LM Kalikin, LA Johnson… - Proceedings of the …, 1995 - National Acad Sciences
Beckwith-Wiedemann syndrome (BWS) involves fetal overgrowth and predisposition to a
wide variety of embryonal tumors of childhood. We have previously found that BWS is …

[PDF][PDF] Isolation and characterization of the human SCP2 cDNA and chromosomal localization of the gene.

JA Schalk, HH Offenberg, E Peters, NP Groot… - SCP2, a major protein …, 1999 - library.wur.nl
SCP2 is a meiosis-specific component of the axial elements of synaptonemal complexes,
and was originally identified in the rat. The cDNA encoding SCP2 of the rat (rnSCP2) has …

Further delineation of the partial proximal trisomy 10q syndrome.

CM Aalfs, JM Hoovers, MA Nieste-Otter… - Journal of medical …, 1995 - jmg.bmj.com
We report on a girl with a partial duplication of the proximal part of the long arm of
chromosome 10, confirmed by chromosome painting. The phenotypic findings are compared …

Fluorescence in situ hybridization in the study of chromosomal abnormalities

JM Hoovers, CH Mellink, NJ Leschot - Nederlands Tijdschrift voor …, 1999 - europepmc.org
Classical cytogenetics has a low resolving power and allows analysis of dividing cells only.
In fluorescence in situ hybridization (FISH), a DNA fragment is stained with a fluorescent …

Flow cytometric detection of chromosome abnormalities by measuring centromeric index, DNA content, and DNA base composition.

W Rens, GA Boschman, JM Hoovers… - … : the Journal of the …, 1994 - europepmc.org
This paper highlights two improvements of the on-line centromeric index (CI) analysis for the
detection of chromosome abnormalities. On-line CI versus DNA content analysis of an EBV …

[PDF][PDF] Association between Y-chromosomal haplotypes and susceptibility to Barrett's esophagus

AM Rygiel, S Repping, WM Westra… - Genetic markers in …, 2008 - dare.uva.nl
ABSTRACT Background & Aims: Barrett's esophagus (BE) is a metaplastic condition of the
distal esophagus, which predisposes for esophageal adenocarcinoma (EAC). It is believed …

[CITATION][C] Holoprosencephaly associated with ring chromosome 21

JM Hoovers, MC Jansweijer - Clinical genetics, 1987 - pubmed.ncbi.nlm.nih.gov