Inner ear and kidney anomalies caused by IAP insertion in an intron of the Eya1 gene in a mouse model of BOR syndrome

By Erway L.C.  

Human Molecular Genetics, Vol. 8, Iss. 4, 1999-04 ,pp. : 645-653

Oxford University Press

Access to resources Recommend Favorite

Prenatal and postnatal development of the mammalian ear

By  

Birth Defects Research, Vol. 110, Iss. 3, 2018-02 ,pp. : 228-245

John Wiley & Sons Inc

Access to resources Recommend Favorite

Mutation of the novel gene Tmie results in sensory cell defects in the inner ear of spinner, a mouse model of human hearing loss DFNB6

By Mitchem K.L.  

Human Molecular Genetics, Vol. 11, Iss. 16, 2002-08 ,pp. : 1887-1898

Oxford University Press

Access to resources Recommend Favorite

A specific promoter of the sensory cells of the inner ear defined by transgenesis

By Boëda B.   Weil D.   Petit C.  

Human Molecular Genetics, Vol. 10, Iss. 15, 2001-07 ,pp. : 1581-1589

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