Baseline connectome modular abnormalities in the childhood phase of a longitudinal study on individuals with chromosome 22q11.2 deletion syndrome

Occurring in at least 1 in 3,000 live births, chromosome 22q11.2 deletion syndrome (22q11DS) produces a complex phenotype that includes a constellation of medical complications such as congenital cardiac defects, immune deficiency, velopharyngeal dysfunction, and characteristic facial dysmorphic fea...

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Enregistré dans:
Détails bibliographiques
Publié dans:Hum Brain Mapp
Auteurs principaux: Zhan, Liang, Jenkins, Lisanne M., Zhang, Aifeng, Conte, Giorgio, Forbes, Angus, Harvey, Danielle, Angkustsiri, Kathleen, Goodrich‐Hunsaker, Naomi J., Durdle, Courtney, Lee, Aaron, Schumann, Cyndi, Carmichael, Owen, Kalish, Kristopher, Leow, Alex D., Simon, Tony J.
Format: Artigo
Langue:Inglês
Publié: John Wiley and Sons Inc. 2017
Sujets:
Research Articles
Accès en ligne:https://ncbi.nlm.nih.gov/pmc/articles/PMC5757536/
https://ncbi.nlm.nih.gov/pubmed/28990258
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/hbm.23838
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