Related content

The 22q11 deletion syndrome candidate gene Tbx1 determines thyroid size and positioning

By Fagman H.   Liao J.   Westerlund J.   Andersson L.   Morrow B.E.   Nilsson M.  

Human Molecular Genetics, Vol. 16, Iss. 3, 2007-02 ,pp. : 276-285

Oxford University Press

Access to resources Recommend Favorite

Dissection of Tbx1 and Fgf interactions in mouse models of 22q11DS suggests functional redundancy

By Aggarwal Vimla S.   Liao Jun   Schimmang Thomas   Lewandoski Mark   Locker Joseph   Shanske Alan   Campione Marina   Morrow Bernice E.  

Human Molecular Genetics, Vol. 15, Iss. 21, 2006-11 ,pp. : 3219-3228

Oxford University Press

Access to resources Recommend Favorite

Tissue-specific roles of Tbx1 in the development of the outer, middle and inner ear, defective in 22q11DS patients

By Arnold Jelena S.   Braunstein Evan M.   Ohyama Takahiro   Groves Andrew K.   Adams Joe C.   Brown M. Christian   Morrow Bernice E.  

Human Molecular Genetics, Vol. 15, Iss. 10, 2006-05 ,pp. : 1629-1639

Oxford University Press

Access to resources Recommend Favorite

Research sheds light on gene expression differences in 22q11.2 deletion syndrome

By  

American Journal Of Medical Genetics Part A, Vol. 167, Iss. 11, 2015-11 ,pp. : x-xi

John Wiley & Sons Inc

Access to resources Recommend Favorite

Tbx1 regulates oral epithelial adhesion and palatal development

By Funato Noriko   Nakamura Masataka   Richardson James A.   Srivastava Deepak   Yanagisawa Hiromi  

Human Molecular Genetics, Vol. 21, Iss. 11, 2012-06 ,pp. : 2524-2537

Oxford University Press

Access to resources Recommend Favorite