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Delineating the psychiatric and behavioral phenotype of recurrent 2q13 deletions and duplications
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FOXP1-related intellectual disability syndrome : a recognisable entity
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7p22.1 microdeletions involving ACTB associated with developmental delay, short stature, and microcephaly
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Mate pair sequencing for the detection of chromosomal aberrations in patients with intellectual disability and congenital malformations
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Implementation of genomic arrays in prenatal diagnosis: the Belgian approach to meet the challenges