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Microarray analysis of theDf1mouse model of the 22q11 deletion syndrome

โœ Scribed by Katrina Prescott; Sarah Ivins; Mike Hubank; Elizabeth Lindsay; Antonio Baldini; Peter Scambler


Book ID
106134263
Publisher
Springer
Year
2005
Tongue
English
Weight
289 KB
Volume
116
Category
Article
ISSN
0340-6717

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A 27 weeks' gestation fetus, evaluated because of polyhydramnios, was found by echocardiography to have an interrupted aortic arch type B. Because of the known association between this malformation and DiGeorge syndrome, an amniocentesis was performed. Fluorescence in situ hybridization revealed a 2