Tbx22 null mice have a submucous cleft palate due to reduced palatal bone formation and also display ankyloglossia and choanal atresia phenotypes

By Pauws Erwin   Hoshino Aya   Bentley Lucy   Prajapati Suresh   Keller Charles   Hammond Peter   Martinez-Barbera Juan-Pedro   Moore Gudrun E.   Stanier Philip  

Human Molecular Genetics, Vol. 18, Iss. 21, 2009-11 ,pp. : 4171-4179

Oxford University Press

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Craniofacial expression of human and murine TBX22 correlates with the cleft palate and ankyloglossia phenotype observed in CPX patients

By Moore G.E.  

Human Molecular Genetics, Vol. 11, Iss. 22, 2002-10 ,pp. : 2793-2804

Oxford University Press

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Mkks-null mice have a phenotype resembling Bardet–Biedl syndrome

By Fath Melissa A.  

Human Molecular Genetics, Vol. 14, Iss. 9, 2005-05 ,pp. : 1109-1118

Oxford University Press

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Bone density phenotypes in mice aneuploid for the Down syndrome critical region

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American Journal Of Medical Genetics Part A, Vol. 155, Iss. 10, 2011-10 ,pp. : 2436-2445

John Wiley & Sons Inc

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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

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