Structural and Mutational Analysis of a Conserved Gene ( DGSI ) from the Minimal DiGeorge Syndrome Critical Region

By Gong Weilong   Emanuel Beverly S.   Galili Naomi   Kim David H.   Roe Bruce   Driscoll Deborah A.   Budarf Marcia L.  

Human Molecular Genetics, Vol. 6, Iss. 2, 1997-01 ,pp. : 267-276

Oxford University Press

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The Murine Homologue of HIRA, a DiGeorge Syndrome Candidate Gene, Is Expressed in Embryonic Structures Affected in Human CATCH22 Patients

By Wilming Laurens G.   Snoeren C. A. Sylvia   van Rijswijk Angelique   Grosveld Frank   Meijers Carel  

Human Molecular Genetics, Vol. 6, Iss. 2, 1997-01 ,pp. : 247-258

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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Identification of a novel nuclear localization signal in Tbx1 that is deleted in DiGeorge syndrome patients harboring the 1223delC mutation

By Stoller Jason Z.  

Human Molecular Genetics, Vol. 14, Iss. 7, 2005-04 ,pp. : 885-892

Oxford University Press

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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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