Identification of a Tbx1/Tbx2/Tbx3 genetic pathway governing pharyngeal and arterial pole morphogenesis

By Mesbah Karim   Rana M. Sameer   Francou Alexandre   van Duijvenboden Karel   Papaioannou Virginia E.   Moorman Antoon F.   Kelly Robert G.   Christoffels Vincent M.  

Human Molecular Genetics, Vol. 21, Iss. 6, 2012-03 ,pp. : 1217-1229

Oxford University Press

Access to resources Recommend Favorite

The MEF2C-Related and 5q14.3q15 Microdeletion Syndrome

By  

Molecular Syndromology, Vol. 2, Iss. 3-5, 2012-04 ,pp. : 164-170

Karger

Access to resources Recommend Favorite

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

Access to resources Recommend Favorite

TBX1 is required for inner ear morphogenesis

By Vitelli F.   Viola A.   Morishima M.   Pramparo T.   Baldini A.   Lindsay E.  

Human Molecular Genetics, Vol. 12, Iss. 16, 2003-08 ,pp. : 2041-2048

Oxford University Press

Access to resources Recommend Favorite

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

Access to resources Recommend Favorite