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496 results for your search :
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Coffin-Lowry syndrome in female patients: neurodevelopmental and malformative phenotype
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GABPB1 gene in intellectual disability
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Neurodevelopmental phenotypes associated to HSF2 deleterious variation
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Further clinical and genetic characterization of the KDM2B-related disorder
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Expanding the spectrum of the BCAS3-related disorder
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EuroDysmorpho 2023 Photos
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Further clinical and imaging characterisation of ZC4H2 related disorder
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Multidisciplinary Fetal Diagnostics Winter School – 2023 edition
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Multidisciplinary Fetal Diagnostics Winter School – 2023 edition
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ERN-ITHACA Patient Board Meeting