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Neurology|November 18, 1998
Cardiac involvement in genetically confirmed facioscapulohumeral muscular dystrophyP Laforêt, C de Toma, B Eymard, et al.Plastic and Reconstructive Surgery|January 25, 2023
A Contemporary Review of the Role of Facial Prostheses in Complex Facial ReconstructionAllison A Slijepcevic, Azadeh Afshari, Ann E Vitale, et al.Revista Espanola De Cardiologia|March 17, 2006
[Inferior vena cava malformations and deep venous thrombosis]María J García-Fuster, María J Forner, Blas Flor-Lorente, et al.Human Genetics|October 1, 1986
De novo DNA microdeletion in a girl with Turner syndrome and Duchenne muscular dystrophyJ Chelly, F Marlhens, B Le Marec, et al.Journal of Medical Genetics|June 1, 1991
Contribution to carrier detection and genetic counselling in X linked retinoschisisJ Kaplan, A Pelet, H Hentati, et al.Human Molecular Genetics|August 25, 2000
Establishment of the paternal methylation imprint of the human H19 and MEST/PEG1 genes during spermatogenesisA Kerjean, J M Dupont, C Vasseur, et al.Annales De Genetique|January 1, 1988
Duplication of HRAS1, INS, and IGF2 is not a common event in Beckwith-Wiedemann syndromeI Henry, M Jeanpierre, F Barichard, et al.Heart & Lung : the Journal of Critical Care|September 27, 2020
Cardiac sarcoidosis as an incidental finding: A case reportAna Gabaldon-Perez, Sergio Garcia-Blas, Maria J Forner, et al.Neuromuscular Disorders : NMD|March 1, 1994
Expression of dystrophin-associated proteins in dystrophin-positive muscle fibers (revertants) in Duchenne muscular dystrophyK Matsumura, F M Tomé, H Collin, et al.Plos One|September 22, 2015
Increased Urinary Exosomal MicroRNAs in Patients with Systemic Lupus ErythematosusJavier Perez-Hernandez, Maria J Forner, Carolina Pinto, et al.Pageof 1,427