22q11 Deletion Syndrome
Author:
Publisher
Elsevier
Reference14 articles.
1. Clinical experience with single-nucleotide polymorphism-based noninvasive prenatal screening for 22q11.2 deletion syndrome;Gross;Ultrasound Obstet Gynecol,2015
2. Behavioral and psychiatric phenotypes in 22q11.2 deletion syndrome;Tang;J Dev Behav Pediatr,2015
3. Whole-Genome Sequencing Suggests Schizophrenia Risk Mechanisms in Humans with 22q11.2 Deletion Syndrome;Merico;G3 (Bethesda),2015
4. The risk of 22q11.2 deletion in foetuses with a right aortic arch and without intracardiac anomalies;Perolo;Ultrasound Obstet Gynecol,2015
5. Current Status of Testing for Microdeletion Syndromes and Rare Autosomal Trisomies Using Cell-Free DNA Technology;Yaron;Obstet Gynecol,2015
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