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Mieke van Haelst

2PUBLICATIONS

1CO-AUTHORS

Developmental genetics (incl. sex determination)Gene expression (incl. microarray and other genome-wide approaches)

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Publications (2)

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|Nov 27, 2014

Further delineation of the KBG syndrome phenotype caused by ANKRD11 aberrations.

Charlotte W Ockeloen, Marjolein H Willemsen, Sonja de Munnik

|Oct 10, 2013

Mate pair sequencing for the detection of chromosomal aberrations in patients with intellectual disability and congenital malformations.

Sarah Vergult, Ellen Van Binsbergen, Tom Sante

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Edwin Cuppen

Frequent Collaborators

1 joint publications

Edwin Cuppen

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