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A Novel Strategy Combining Array-CGH, Whole-exome Sequencing and In Utero Electroporation in Rodents to Identify Causative Genes for Brain Malformations
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Clinical Manifestations of 22q11.2 Deletion Syndrome

Annapaola Cirillo1, Michele Lioncino1, Annachiara Maratea1

  • 1Inherited and Rare Cardiovascular Disease Unit, Department of Translational Medical Sciences, University of Campania "Luigi Vanvitelli", Via L. Bianchi, 80131 Naples, Italy.

Heart Failure Clinics
|November 15, 2021
PubMed

Keywords:
22q11.2 deletion syndromeAortic arch abnormalitiesConotruncal abnormalitiesDi George syndrome

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