All-cause mortality and survival in adults with 22q11.2 deletion syndrome

PURPOSE: Given limited data available on long-term outcomes in 22q11.2 deletion syndrome (22q11.2DS), we investigated mortality risk in adults with this microdeletion syndrome. METHODS: We studied 309 well-characterized adults (age ≥17 years) with 22q11.2DS and their 1014 unaffected parents and sibl...

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Udgivet i:Genet Med
Main Authors: Van, Lily, Heung, Tracy, Graffi, Justin, Ng, Enoch, Malecki, Sarah, Van Mil, Spencer, Boot, Erik, Corral, Maria, Chow, Eva W. C., Hodgkinson, Kathleen A., Silversides, Candice, Bassett, Anne S.
Format: Artigo
Sprog:Inglês
Udgivet: Nature Publishing Group US 2019
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Article
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC6774995/
https://ncbi.nlm.nih.gov/pubmed/30948858
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41436-019-0509-y
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