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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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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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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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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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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