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September 2008 / Genes Dev Regulation of muscle development by DPF3, a novel histone acetylation and methylation reader of the BAF chromatin remodeling complex M. Lange B. Kaynak U.B. Foerster M. Toenjes J.J. Fischer C. Grimm J. Schlesinger S. Just I. Dunkel T. Krueger S. Mebus H. Lehrach R. Lurz J. Gobom W. Rottbauer S. Abdelilah-Seyfried S. Sperling 01. Januar 2016 Human genetics of defects of situs A. Perrot S. Rickert-Sperling 01. Januar 2016 Human genetics of ventricular septal defect K. Bellmann A. Perrot S. Rickert-Sperling 01. Januar 2016 Preface S. Rickert-Sperling R.G. Kelly D.J. Driscoll 01. Januar 2016 Congenital heart diseases: the broken heart : clinical features, human genetics and molecular pathways S. Rickert-Sperling R.G. Kelly D.J. Driscoll 01. Januar 2016 Cardiac transcription factors and regulatory networks M. Grunert C. Dorn S. Rickert-Sperling 01. Januar 2016 Human genetics of tetralogy of fallot and double outlet right ventricle C. Dorn A. Perrot S. Rickert-Sperling 01. Januar 2016 Technologies to study genetics and molecular pathways C. Dorn M. Grunert A. Dopazo F. Sanchez-Cabo A. Gatto J. Vazquez S. Rickert-Sperling E. Lara-Pezzi 01. März 2013 / Eur J Hum Genet Novel mutations in the sarcomeric protein myopalladin in patients with dilated cardiomyopathy T. Meyer V. Ruppert S. Ackermann A. Richter A. Perrot S.R. Sperling M.G. Posch B. Maisch S. Pankuweit 01. Januar 2014 / Brief Funct Genomics Application of high-throughput sequencing for studying genomic variations in congenital heart disease C. Dorn M. Grunert S.R. Sperling Seitennummerierung Aktuelle Seite 1 Seite 2 Seite 3 Seite 4 … Nächste Seite Next › Letzte Seite Last »
01. September 2008 / Genes Dev Regulation of muscle development by DPF3, a novel histone acetylation and methylation reader of the BAF chromatin remodeling complex M. Lange B. Kaynak U.B. Foerster M. Toenjes J.J. Fischer C. Grimm J. Schlesinger S. Just I. Dunkel T. Krueger S. Mebus H. Lehrach R. Lurz J. Gobom W. Rottbauer S. Abdelilah-Seyfried S. Sperling
01. Januar 2016 Human genetics of ventricular septal defect K. Bellmann A. Perrot S. Rickert-Sperling
01. Januar 2016 Congenital heart diseases: the broken heart : clinical features, human genetics and molecular pathways S. Rickert-Sperling R.G. Kelly D.J. Driscoll
01. Januar 2016 Cardiac transcription factors and regulatory networks M. Grunert C. Dorn S. Rickert-Sperling
01. Januar 2016 Human genetics of tetralogy of fallot and double outlet right ventricle C. Dorn A. Perrot S. Rickert-Sperling
01. Januar 2016 Technologies to study genetics and molecular pathways C. Dorn M. Grunert A. Dopazo F. Sanchez-Cabo A. Gatto J. Vazquez S. Rickert-Sperling E. Lara-Pezzi
01. März 2013 / Eur J Hum Genet Novel mutations in the sarcomeric protein myopalladin in patients with dilated cardiomyopathy T. Meyer V. Ruppert S. Ackermann A. Richter A. Perrot S.R. Sperling M.G. Posch B. Maisch S. Pankuweit
01. Januar 2014 / Brief Funct Genomics Application of high-throughput sequencing for studying genomic variations in congenital heart disease C. Dorn M. Grunert S.R. Sperling