Mieke van Haelst
0000-0002-7519-0246
4 papers found
Refreshing results…
Evaluation of 100 Dutch cases with 16p11.2 deletion and duplication syndromes; from clinical manifestations towards personalized treatment options
Novel PUF60 variant suggesting an interaction between Verheij and Cornelia de Lange syndrome: phenotype description and review of the literature
The neurodevelopmental and facial phenotype in individuals with a TRIP12 variant
Mate pair sequencing for the detection of chromosomal aberrations in patients with intellectual disability and congenital malformations
Missing publications? Search for publications with a matching author name.