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Implementation of fetal clinical exome sequencing : comparing prospective and retrospective cohorts
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Performance and diagnostic value of genome-wide noninvasive prenatal testing in multiple gestations
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Prenatally detected copy number variants in a national cohort : a postnatal follow-up study
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Defining the clinical, molecular and imaging spectrum of adaptor protein complex 4-associated hereditary spastic paraplegia
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Biallelic B3GALT6 mutations cause spondylodysplastic Ehlers-Danlos syndrome
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The Belgian MicroArray Prenatal (BEMAPRE) database : a systematic nationwide repository of fetal genomic aberrations
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Implementation of genomic arrays in prenatal diagnosis: the Belgian approach to meet the challenges
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Exonic deletions in AUTS2 cause a syndromic form of intellectual disability and suggest a critical role for the C terminus