The phenotypic spectrum of terminal 6q deletions based on a large cohort derived from social media and literature: a prominent role for DLL1

Overview of attention for article published in Orphanet Journal of Rare Diseases, March 2023

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RT @AafkeEngwerda: Our paper on the phenotypic spectrum of terminal 6q deletions is out now! We were able to identify 38 new individuals an…

RT @CRavenswaaij: Proud on my #chromosome6 project team! A third paper is coming up soon. A big thank you to all families involved! @UMCG…

RT @CRavenswaaij: Proud on my #chromosome6 project team! A third paper is coming up soon. A big thank you to all families involved! @UMCG…

RT @AafkeEngwerda: You can read more about terminal 6q deletions in our publication on the phenotypic spectrum here: https://t.co/RKNYDf88l2

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