Eya1 gene dosage critically affects the development of sensory epithelia in the mammalian inner ear

By Zou Dan   Erickson Christopher   Kim Eun-Hee   Jin Dongzhu   Fritzsch Bernd   Xu Pin-Xian  

Human Molecular Genetics, Vol. 17, Iss. 21, 2008-11 ,pp. : 3340-3356

Oxford University Press

Access to resources Recommend Favorite

Molecular effects of Eya1 domain mutations causing organ defects in BOR syndrome

By Buller C.   Xu X.   Marquis V.   Schwanke R.   Xu P-X.  

Human Molecular Genetics, Vol. 10, Iss. 24, 2001-11 ,pp. : 2775-2781

Oxford University Press

Access to resources Recommend Favorite

HIGM syndrome caused by insertion of an AluYb8 element in exon 1 of the CD40LG gene

By Apoil P.   Kuhlein E.   Robert A.   Rubie H.   Blancher A.  

Immunogenetics, Vol. 59, Iss. 1, 2007-01 ,pp. : 17-23

Springer Publishing Company

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

Mouse Pale Ear (ep) is Homologous to Human Hermansky-Pudlak Syndrome and Contains a Rare ‘AT-AC’ Intron

By Feng Guo Hong   Bailin Tu   Oh Jangsuk   Spritz Richard A.  

Human Molecular Genetics, Vol. 6, Iss. 5, 1997-01 ,pp. : 793-797

Oxford University Press

Access to resources Recommend Favorite