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Facial features in children with the 22q11 deletion syndrome

✍ Scribed by S Óskarsdóttir; E Holmberg; A Fasth; K Strömland


Book ID
114815614
Publisher
John Wiley and Sons
Year
2008
Tongue
English
Weight
392 KB
Volume
97
Category
Article
ISSN
0803-5253

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## Abstract The 22q11 chromosomal deletion syndrome (22q11DS) is associated with a heterogeneous physical phenotype, neurocognitive deficits, and increased risk of later psychiatric illness. Sporadic clinical reports suggested motor differences, but quantitative studies of movement in children with