Mice overexpressing genes from the 22q11 region deleted in velo-cardio-facial syndrome/DiGeorge syndrome have middle and inner ear defects

By Schüler T.  

Human Molecular Genetics, Vol. 10, Iss. 22, 2001-10 ,pp. : 2549-2556

Oxford University Press

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Mice deleted for the DiGeorge/velocardiofacial syndrome region show abnormal sensorimotor gating and learning and memory impairments

By Paylor R.  

Human Molecular Genetics, Vol. 10, Iss. 23, 2001-11 ,pp. : 2645-2650

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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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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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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