Non-coding deletions identify Maenli lncRNA as a limb-specific En1 regulator
Lila Allou(NIHR Imperial Biomedical Research Centre), Andrea Superti‐Furga(University of Lausanne), Luciano Farage(Instituto de Cardiologia do Distrito Federal), Phillip Grote(Goethe University Frankfurt), Florence Niel‐Bütschi(University of Lausanne), Andreas Magg(Max Planck Institute for Molecular Genetics), Belinda Campos‐Xavier(University of Lausanne), Stefan Mundlos(Humboldt-Universität zu Berlin), Sheela Nampoothiri(Amrita Institute of Medical Sciences and Research Centre), Cesar A. Prada‐Medina(Max Planck Institute for Molecular Genetics), Charles Marques Lourenço(Universidade de São Paulo), Robert Schöpflin(Max Planck Institute for Molecular Genetics), Srilakshmi Rajagopal(Tamil Nadu Dr. M.G.R. Medical University), Bernd Timmermann(Max Planck Institute for the Study of Societies), Guillaume Andrey(Max Planck Institute for Molecular Genetics), Michael I. Robson(Max Delbrück Center), Wing-Lee Chan(Charité - Universitätsmedizin Berlin), Malte Spielmann(Christian-Albrechts-Universität zu Kiel), Verena Heinrich(Max Planck Institute for Molecular Genetics), Sara Balzano(University of Verona), Luisa Bonafé(University of Lausanne), Rosanna Pescini Gobert(University of Lausanne), Carole Chiesa(University of Lausanne), Daniel R. Carvalho(Areté Associates (United States)), Alessa R. Ringel(Max Planck Institute for Molecular Genetics), Mathieu Quinodoz(University of Leicester), Sheila Unger(University of Lausanne), Giulia Cova(New York University), Lars Wittler(Max Planck Institute for Molecular Genetics), Regina Albuquerque(Faculdade de Medicina de São José do Rio Preto), Béryl Royer‐Bertrand(University of Lausanne), Carlos E. Speck‐Martins(Sarah Network of Rehabilitation Hospitals), Carlo Rivolta(University of Lausanne)
Cited by 119
Related Papers
The single-cell transcriptional landscape of mammalian organogenesis
|Nature|2019|4.7k
Nosology and classification of genetic skeletal disorders: 2010 revision
|American Journal of Medical Genetics Part A|2011|717
Nosology and classification of genetic skeletal disorders: 2019 revision
|American Journal of Medical Genetics Part A|2019|620