Michel Vekemans
Hôpital Necker-Enfants Malades(FR)Inserm(FR)Institut Necker Enfants Malades(FR)
Publications by Year
Research Areas
Genomic variations and chromosomal abnormalities, Genetics and Neurodevelopmental Disorders, Autism Spectrum Disorder Research, Chromosomal and Genetic Variations, Cancer-related molecular mechanisms research
Most-Cited Works
- → Array-based comparative genomic hybridisation identifies high frequency of cryptic chromosomal rearrangements in patients with syndromic autism spectrum disorders(2006)304 cited
- → Neurological Phenotype in Waardenburg Syndrome Type 4 Correlates with Novel SOX10 Truncating Mutations and Expression in Developing Brain(2000)168 cited
- → 19q13.11 deletion syndrome: a novel clinically recognisable genetic condition identified by array comparative genomic hybridisation(2009)81 cited
- → Expression of theRET proto-oncogene in human Embryos(1998)64 cited
- → Ebstein anomaly associated with rearrangements of chromosomal region 11q(1998)32 cited
- → A new lethal syndrome of exomphalos, short limbs, and macrogonadism(1999)3 cited
- → Characterization of a Region-Specific Library of Microclones in the Vicinity of the Bcg and splotch Loci on Mouse Chromosome 1(1994)2 cited