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

Molecular effects of calcium binding mutations in Marfan syndrome depend on domain context

By McGettrick Aileen J.   Knott Vroni   Willis Anthony   Handford Penny A.  

Human Molecular Genetics, Vol. 9, Iss. 13, 2000-08 ,pp. : 1987-1994

Oxford University Press

Access to resources Recommend Favorite

FOXD1 Duplication Causes Branchial Defects and Interacts with the TFAP2A Gene Implicated in the Branchio-Oculo-Facial Syndrome in Causing Eye Effects in Zebrafish

By  

Molecular Syndromology, Vol. 1, Iss. 5, 2011-05 ,pp. : 255-261

Karger

Access to resources Recommend Favorite

Structural and functional analyses of disease-causing missense mutations in the forkhead domain of FOXC1

By Saleem Ramsey A.  

Human Molecular Genetics, Vol. 12, Iss. 22, 2003-11 ,pp. : 2993-3005

Oxford University Press

Access to resources Recommend Favorite

The spectrum of mutations in UBE3A causing Angelman syndrome

By Meijers-Heijboer H.  

Human Molecular Genetics, Vol. 8, Iss. 1, 1999-01 ,pp. : 129-135

Oxford University Press

Access to resources Recommend Favorite