22q11.2 Deletion Syndrome: Symptoms, Diagnosis, Treatment

The article analyzes the consequences of chromosomal abnormalities caused by the deletion of a small piece of chromosome 22. This syndrome results in diverse clinical manifestations: congenital heart defects, abnormalities in the large vessels, congenital defects in the maxillofacial area, as well a...

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Main Authors: Leyla S. Namazova-Baranova (Author), Olga V. Ginter (Author), Tatyana A. Polunina (Author), Irina V. Davydova (Author), Kirill V. Savostyanov (Author), Alexandr A. Pushkov (Author), Natalya V. Jourkova (Author), Tatyana Y. Mospan (Author)
Format: Knjiga
Izdano: "Paediatrician" Publishers LLC, 2016-12-01T00:00:00Z.
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