Calls for Collaboration
Download here the template to submit your call by email to the coordination team
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April 19, 2021
CAMK2A-related neurodevelopmental disorder – description of the clinical and neurological phenotype
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April 14, 2021
Implication of missense variants in the NSD1 gene in Sotos-like phenotype
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April 13, 2021
TRIP12-associated neurodevelopmental disorder
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April 12, 2021
ZBTB47/ZNF651 variants
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April 7, 2021
Expanding the phenotype related to de novo missense variants in HNRNPH2
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April 2, 2021
Correlation between intellectual disability and cutaneous skin mosaicism
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March 22, 2021
Clinical and molecular characterization of a novel MYCN related syndrome – A mirror phenotype and molecular of the Feingold syndrome
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March 15, 2021
B4GALT5 as potential candidate gene for a novel sphingolipid disorder
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March 3, 2021
RAB10: a candidate gene for a severe neurodevelopmental syndrome
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February 8, 2021
CHAMP1 clinical spectrum (MRD40 – OMIM 616579)