A new spontaneous mouse mutation of Hoxd13 with a polyalanine expansion and phenotype similar to human synpolydactyly

By Johnson K.R.   Sweet H.O.   Donahue L.R.   Ward-Bailey P.   Bronson R.T.   Davisson M.T.  

Human Molecular Genetics, Vol. 7, Iss. 6, 1998-06 ,pp. : 1033-1038

Oxford University Press

Access to resources Recommend Favorite

Cardiovascular defects in a mouse model of HOXA1 syndrome

By Makki Nadja   Capecchi Mario R.  

Human Molecular Genetics, Vol. 21, Iss. 1, 2012-01 ,pp. : 26-31

Oxford University Press

Access to resources Recommend Favorite

Genomic Structure of HOXD13 Gene: A Nine Polyalanine Duplication Causes Synpolydactyly in Two Unrelated Families

By Akarsu A. Nurten   Stoilov Ivaylo   Yilmaz Engin   Sayli B. Sitki   Sarfarazi Mansoor  

Human Molecular Genetics, Vol. 5, Iss. 7, 1996-01 ,pp. : 945-952

Oxford University Press

Access to resources Recommend Favorite

Deleterious and protective properties of an aggregate-prone protein with a polyalanine expansion

By Berger Zdenek   Davies Janet E.   Pasco Matthieu Y.   Majoul Irina   O'Kane Cahir J.  

Human Molecular Genetics, Vol. 15, Iss. 3, 2006-02 ,pp. : 453-465

Oxford University Press

Access to resources Recommend Favorite

Differential effects of a polyalanine tract expansion in Arx on neural development and gene expression

By Nasrallah MacLean Pancoast   Cho Ginam   Simonet Jacqueline C.   Putt Mary E.   Kitamura Kunio   Golden Jeffrey A.  

Human Molecular Genetics, Vol. 21, Iss. 5, 2012-03 ,pp. : 1090-1098

Oxford University Press

Access to resources Recommend Favorite