Calls for Collaboration
Download here the template to submit your call by email to the coordination team
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August 16, 2021
CTNNA3 microdeletion: a description of clinical features
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August 9, 2021
Development of a DNA methylation episignature for variants in KDM3
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August 4, 2021
KBG syndrome evolving phenotype
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August 2, 2021
CTNNA3 microdeletion: a description of clinical features
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August 2, 2021
A novel X-linked syndromic neurodevelopmental disorders associated with WDR44 pathogenic variants
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August 2, 2021
TRA2B-associated neurodevelopmental delay
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July 19, 2021
De novo missense variants in EIF3I cause a novel neurodevelopmental disorder with midline brain defects and skeletal abnormalities
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July 13, 2021
Search for patients harbouring a de novo heterozygous variant in SP9 gene
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June 28, 2021
FOREIGN (FOSL2-related signs)
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June 28, 2021
POGZ variants in neurodevelopmental disorders