ECARUCA Research Platforms
Within the Microdeletion/duplication Research Network (MRN) we aim to set up new collaborative studies, which might help a thorough clinical
analysis of patients with overlapping chromosome aberrations and to pin point the
gene(s) responsible for the phenotype. All relevant results will be included into the ECARUCA
database in order to make them available to the European scientific community. Please use the links below for more information concerning
specific research projects.
subtelomeric 1q imbalances
subtelomeric 9qter imbalances
subtelomeric 10qter imbalances
subtelomeric 18qter imbalances
FP6 AnEUploidy project (See also
www.aneuploidy.eu
for additional information)
Patients with a partial trisomy or monosomy of chromosome 21: Chromosome 21 AnEUploidy
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