Contents Vol. 4, 2013
Martin Poot(Wageningen University & Research), Sandra Mercier(Centre Hospitalier Universitaire de Nantes), Dominique Martin‐Coignard(Centre Hospitalier du Mans), C. de Campos Legnaro, Florence Démurger(Centre hospitalier Bretagne Atlantique), Rocio Ortı́z-López, R. Brian Lowry(Alberta Health Services), Augusto Rojas-Martı́nez(Universidad Autónoma de Nuevo León), Julia Tantau, Arash Ghalamkarpour, Lucilene Arilho Ribeiro(Universidade de São Paulo), S. Jaillard, Laurent Pasquier(Institut de génétique et de développement de Rennes), Elodie Fastré, Isabelle Gicquel, Carlos Córdova‐Fletes, Valérie Dupé(Centre National de la Recherche Scientifique), Dávid Jónás, J. Lespinasse(Centre Hospitalier Métropole Savoie), Dagmar Weise(Altonaer Kinderkrankenhaus), Olaf Bartsch, Leslie Ratié, Lizeth Martínez‐Jacobo, U. Zechner, Alexandre Irrthum, C. Saucedo-Carrasco, B. Leheup, Mylène Béri, Matthieu J. Schlögel, Nicolas Chassaing(Université Fédérale de Toulouse Midi-Pyrénées), J.P.H. Wyse, T. Haaf, C. Evain, R.M. Candido Sandri, Josseline Kaplan(Inserm), C. Dubourg(Centre National de la Recherche Scientifique), Ha‐Long Nguyen(de Duve Institute), Conny M.A. van Ravenswaaij‐Arts(University Medical Center Groningen), M.S. Connelly, J. Peter van Tintelen(Utrecht University), E. Burgdörfer, Fernando Rivas, Bruno Faulin Gamba, N. Corsten-Janssen, A. Richieri‐Costa, O. Patat, T. Dijkhuizen, Judy Chernos, M. Korenkov, Antonella Mendola(de Duve Institute)
Cited by 0
Related Papers
2023 ESC Guidelines for the management of cardiomyopathies
|European Heart Journal|2023|2.3k
Interferon Regulatory Factor 6 ( <i>IRF6</i> ) Gene Variants and the Risk of Isolated Cleft Lip or Palate
|New England Journal of Medicine|2004|583
Risk Factors for Malignant Ventricular Arrhythmias in Lamin A/C Mutation Carriers
|Journal of the American College of Cardiology|2012|519
Genetic and Functional Analyses of SHANK2 Mutations Suggest a Multiple Hit Model of Autism Spectrum Disorders
|PLoS Genetics|2012|443
Choreoathetosis, hypothyroidism, and pulmonary alterations due to human NKX2-1 haploinsufficiency
|Journal of Clinical Investigation|2002|311