Bert B A de Vries

An update on ECARUCA, the European Cytogeneticists Association Register of Unbalanced Chromosome Aberrations.

Nicole de Leeuw, Jayne Y Hehir-Kwa, A. V. Vulto-van Silfhout, 2013, European journal of medical genetics.

Array-based comparative genomic hybridization for the genomewide detection of submicroscopic chromosomal abnormalities.

Ton Feuth, Kazutoyo Osoegawa, Han G Brunner, 2003, American journal of human genetics.

Diagnostic genome profiling: unbiased whole genome or targeted analysis?

B. D. de Vries, J. Veltman, Bert B A de Vries, 2006, The Journal of molecular diagnostics : JMD.

Loss-of-function mutations in euchromatin histone methyl transferase 1 (EHMT1) cause the 9q34 subtelomeric deletion syndrome.

Alex Magee, Erik A Sistermans, Jean-Pierre Fryns, 2006, American journal of human genetics.

ZNF674: a new kruppel-associated box-containing zinc-finger gene involved in nonsyndromic X-linked mental retardation.

Sander B Nabuurs, Lionel Willatt, Jamel Chelly, 2006, American journal of human genetics.

The genomic landscape of balanced cytogenetic abnormalities associated with human congenital anomalies

Edwin Cuppen, Claire Redin, Ryan L. Collins, 2016, Nature Genetics.

Diagnostic genome profiling in mental retardation.

Ton Feuth, Martijn A. R. Leisink, Erik A Sistermans, 2005, American journal of human genetics.