๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

A candidate gene approach to identify modifiers of the palatal phenotype in 22q11.2 deletion syndrome patients

โœ 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

No coin nor oath required. For personal study only.


๐Ÿ“œ SIMILAR VOLUMES


Candidate genes and the behavioral pheno
โœ Sarah E. Prasad; Sarah Howley; Kieran C. Murphy ๐Ÿ“‚ Article ๐Ÿ“… 2008 ๐Ÿ› Wiley (John Wiley & Sons) ๐ŸŒ English โš– 154 KB

## 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

Evaluation of potential modifiers of the
โœ Elizabeth Goldmuntz; Deborah A. Driscoll; Beverly S. Emanuel; Donna McDonald-McG ๐Ÿ“‚ Article ๐Ÿ“… 2009 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 76 KB

## 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