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Angela Sobotka

Baylor College of Medicine

3

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329

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Genetic dissection of behavioural abnormalities in mouse models of DiGeorge/velocardiofacial syndrome

2006 Journal of Intellectual Disability Research
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Fgf8 expression in the Tbx1 domain causes skeletal abnormalities and modifies the aortic arch but not the outflow tract phenotype of Tbx1 mutants.

2006 Developmental Biology
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Tbx1 haploinsufficiency is linked to behavioral disorders in mice and humans: Implications for 22q11 deletion syndrome

2006 Proceedings of the National Academy of Sciences of the United States of America
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