Related content

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

A G220V substitution within the N-terminal transcription regulating domain of HOXD13 causes a variant synpolydactyly phenotype

By Fantini Sebastian   Vaccari Giulia   Brison Nathalie   Debeer Philippe   Tylzanowski Przemko   Zappavigna Vincenzo  

Human Molecular Genetics, Vol. 18, Iss. 5, 2009-03 ,pp. : 847-860

Oxford University Press

Access to resources Recommend Favorite

Polyalanine expansion in HOXA13: three new affected families and the molecular consequences in a mouse model

By Innis Jeffrey W.  

Human Molecular Genetics, Vol. 13, Iss. 22, 2004-11 ,pp. : 2841-2851

Oxford University Press

Access to resources Recommend Favorite

An N-terminal G11A mutation in HOXD13 causes synpolydactyly and interferes with Gli3R function during limb pre-patterning †

By Brison Nathalie   Debeer Philippe   Fantini Sebastian   Oley Christine   Zappavigna Vincenzo   Luyten Frank P.   Tylzanowski Przemko  

Human Molecular Genetics, Vol. 21, Iss. 11, 2012-06 ,pp. : 2464-2475

Oxford University Press

Access to resources Recommend Favorite

The Friedreich ataxia GAA repeat expansion mutation induces comparable epigenetic changes in human and transgenic mouse brain and heart tissues

By Al-Mahdawi Sahar   Pinto Ricardo Mouro   Ismail Ozama   Varshney Dhaval   Lymperi Stefania   Sandi Chiranjeevi   Trabzuni Daniah   Pook Mark  

Human Molecular Genetics, Vol. 17, Iss. 5, 2008-03 ,pp. : 735-746

Oxford University Press

Access to resources Recommend Favorite