Screening of copy number variants in the 22q11.2 region of congenital heart disease patients from the São Miguel Island, Azores, revealed the second patient with a triplication

Overview of attention for article published in BMC Genomic Data, November 2014

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RT @22qAwarenessDay: Triplications of 22q11.2, share characteristic features with del & dup syndromes but present more severe phenotype htt…

RT @22qAwarenessDay: Triplications of 22q11.2, share characteristic features with del & dup syndromes but present more severe phenotype htt…

RT @22qAwarenessDay: Triplications of 22q11.2, share characteristic features with del & dup syndromes but present more severe phenotype htt…

Triplications of 22q11.2, share characteristic features with del & dup syndromes but present more severe phenotype https://t.co/mqXuELv2j9

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