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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Catatonia in an adolescent with velo‐cardio‐facial syndrome

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American Journal Of Medical Genetics Part A, Vol. 167, Iss. 9, 2015-09 ,pp. : 2150-2153

John Wiley & Sons Inc

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Isolation of a New Clathrin Heavy Chain Gene with Muscle-Specific Expression from the Region Commonly Deleted in Velo-cardio-facial Syndrome

By Sirotkin Howard  

Human Molecular Genetics, Vol. 5, Iss. 5, 1996-01 ,pp. : 617-624

Oxford University Press

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Deletion of 150 kb in the minimal DiGeorge/velocardiofacial syndrome critical region in mouse

By Kimber Wendy L.  

Human Molecular Genetics, Vol. 8, Iss. 12, 1999-11 ,pp. : 2229-2237

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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