Testing criteria for 22q11.2 deletion syndrome: preliminary results of a low cost strategy for public health

Overview of attention for article published in Orphanet Journal of Rare Diseases, June 2019

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facebook: 3 Facebook pages

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So far, Altmetric has seen 10 X posts from 7 X users, with an upper bound of 12,326 followers.

RT @22Q11_Ireland: 22qDS most frequent clinical signs: congenital heart disorders (mainly conotruncal defects), palatal anomalies, hypocalc…

22 Feb 2020

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Twittersphere.... academics and researchers - how many rare chromosomal conditions have these symptoms common across the board? Am guessing quite a few but need some evidence to back up.

21 Feb 2020

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RT @22Q11_Ireland: 22qDS most frequent clinical signs: congenital heart disorders (mainly conotruncal defects), palatal anomalies, hypocalc…

21 Feb 2020

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RT @22Q11_Ireland: 22qDS most frequent clinical signs: congenital heart disorders (mainly conotruncal defects), palatal anomalies, hypocalc…

21 Feb 2020

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