Molecular analysis of the PDS gene in Pendred syndrome (sensorineural hearing loss and goitre)

By Phelps P.D.  

Human Molecular Genetics, Vol. 7, Iss. 7, 1998-07 ,pp. : 1105-1112

Oxford University Press

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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

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Functional differences of the PDS gene product are associated with phenotypic variation in patients with Pendred syndrome and non-syndromic hearing loss (DFNB4)

By Scott Daryl A.   Wang Rong  

Human Molecular Genetics, Vol. 9, Iss. 11, 2000-07 ,pp. : 1709-1715

Oxford University Press

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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

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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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