Deep Phenotyping of Development, Communication and Behaviour in Phelan-McDermid Syndrome
Author:
Publisher
S. Karger AG
Subject
Genetics(clinical),Genetics
Reference26 articles.
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3. Bonaglia M, Giorda R, Beri S, De Agostinil C, Novara F, et al: Molecular mechanisms generating and stabilizing terminal 22q13 deletions in 44 subjects with Phelan-McDermid syndrome. PLoS Genet 7:e1002173 (2011).
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