Cyp26 genes a1, b1 and c1 are down-regulated in Tbx1 null mice and inhibition of Cyp26 enzyme function produces a phenocopy of DiGeorge Syndrome in the chick

By Roberts Catherine   Ivins Sarah   Cook Andrew C.   Baldini Antonio   Scambler Peter J.  

Human Molecular Genetics, Vol. 15, Iss. 23, 2006-12 ,pp. : 3394-3410

Oxford University Press

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A Boy with Holt-Oram Syndrome Caused by Novel Mutation c.1304delT in the TBX5 Gene

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Molecular Syndromology, Vol. 1, Iss. 6, 2011-08 ,pp. : 307-310

Karger

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Isolation of a Novel Gene from the DiGeorge Syndrome Critical Region with Homology to Drosophila gdl and to Human LAMC1 Genes

By Demczuk Suzanne   Thomas Gilles   Aurias Alain  

Human Molecular Genetics, Vol. 5, Iss. 5, 1996-01 ,pp. : 633-638

Oxford University Press

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ES2 , a gene deleted in DiGeorge syndrome, encodes a nuclear protein and is expressed during early mouse development, where it shares an expression domain with a Goosecoid-like gene

By Harvey E.L.  

Human Molecular Genetics, Vol. 7, Iss. 4, 1998-04 ,pp. : 629-635

Oxford University Press

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Recovery from arterial growth delay reduces penetrance of cardiovascular defects in mice deleted for the DiGeorge syndrome region

By Lindsay E.A.   Baldini A.  

Human Molecular Genetics, Vol. 10, Iss. 9, 2001-04 ,pp. : 997-1002

Oxford University Press

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