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502 results for your search :
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SF1 variants in neurodevelopmental disorders
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“Genome architecture: the 16p11.2 rearrangements” by Pr Alexandre Reymond
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“Angelman Syndrome: Past and Present” by Pr Jill Clayton-Smith
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“Genetic & Epigenetic Control of Limb Development and its Anomalies” by Pr Florence Petit
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Eurodysmorpho 2021 Bekim Sadikovic : Fundamental phenotypes in Mendelian neurodevelopmental disorder
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KDM4B gene: clinical phenotype and methylation signature
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Defining Myhre syndrome in Adulthood
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Mild phenotype of EEF1A2 variants
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A novel neurodevelopmental disorders associated with heterozygous DLX1 variants
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Further delineation of the phenotypic spectrum associated to BMP4 pathogenic variants