Missense mutations in the most ancient residues of the PAX6 paired domain underlie a spectrum of human congenital eye malformations

By Hanson I.  

Human Molecular Genetics, Vol. 8, Iss. 2, 1999-02 ,pp. : 165-172

Oxford University Press

Access to resources Recommend Favorite

Reciprocal Effect of Waardenburg Syndrome Mutations on DNA Binding by the Pax-3 Paired Domain and Homeodomain

By Fortin Anouk S.   Underhill D. Alan   Gros Philippe  

Human Molecular Genetics, Vol. 6, Iss. 11, 1997-10 ,pp. : 1781-1790

Oxford University Press

Access to resources Recommend Favorite

A novel missense mutation in the paired domain of PAX9 causes non-syndromic oligodontia

By Jumlongras Dolrudee   Lin Jenn-Yih   Chapra Anas   Seidman Christine   Seidman Jonathan   Maas Richard   Olsen Bjorn  

Human Genetics, Vol. 114, Iss. 3, 2004-02 ,pp. : 242-249

Springer Publishing Company

Access to resources Recommend Favorite

Functional Analysis of Paired Box Missense Mutations in The PAX6 Gene

By Kejun Tang Hank   Chao Lian-Yu   Saunders Grady F.  

Human Molecular Genetics, Vol. 6, Iss. 3, 1997-01 ,pp. : 381-386

Oxford University Press

Access to resources Recommend Favorite

Molecular modeling of retinoschisin with functional analysis of pathogenic mutations from human X-linked retinoschisis

By Sergeev Y.V.   Caruso R.C.   Meltzer M.R.   Smaoui N.   MacDonald I.M.   Sieving P.A.  

Human Molecular Genetics, Vol. 19, Iss. 7, 2010-04 ,pp. : 1302-1313

Oxford University Press

Access to resources Recommend Favorite