## Abstract There is an overwhelming evidence that children and adults with 22q11.2 deletion syndrome (22q11.2DS) have a characteristic behavioral phenotype. In particular, there is a growing body of evidence that indicates an unequivocal association between 22q11.2DS and schizophrenia, especially
โฆ LIBER โฆ
A candidate gene approach to identify modifiers of the palatal phenotype in 22q11.2 deletion syndrome patients
โ Scribed by Josine C.C. Widdershoven; Mark Bowser; Molly B. Sheridan; Donna M. McDonald-McGinn; Elaine H. Zackai; Cynthia B. Solot; Richard E. Kirschner; Frits A. Beemer; Bernice E. Morrow; Marcella Devoto; Beverly S. Emanuel
- Book ID
- 118454579
- Publisher
- Elsevier Science
- Year
- 2013
- Tongue
- English
- Weight
- 180 KB
- Volume
- 77
- Category
- Article
- ISSN
- 0165-5876
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## Abstract ## BACKGROUND: The phenotype associated with deletion of the 22q11.2 chromosomal region is highly variable, yet little is known about the source of this variability. Cardiovascular anomalies, including tetralogy of Fallot, truncus arteriosus, interrupted aortic arch type B, perimembran
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