Best practice guidelines on genetic diagnostics of facioscapulohumeral muscular dystrophy: Update of the 2012 guidelinesEmiliano Giardina, Richard J.L.F. Lemmers, Pilar Camaño et al.|Clinical Genetics|2024Cited by 43
Neuromuscular disease genetics in under-represented populations: increasing data diversityLindsay A. Wilson, Michelle Kvalsund, William L. Macken et al.|Brain|2023Cited by 31
High-resolution breakpoint junction mapping of proximally extended D4Z4 deletions in FSHD1 reveals evidence for a founder effectRichard J.L.F. Lemmers, Silvère M. van der Maarel, Sabrina Sacconi et al.|Human Molecular Genetics|2021Cited by 17
Author response for "Best practice guidelines on genetic diagnostics of facioscapulohumeral muscular dystrophy: Update of the 2012 guidelines"Emiliano Giardina, Richard J.L.F. Lemmers, Pilar Camaño et al.|Unknown|2024Cited by 0
Author response for "Best practice guidelines on genetic diagnostics of facioscapulohumeral muscular dystrophy: Update of the 2012 guidelines"Emiliano Giardina, Richard J.L.F. Lemmers, Pilar Camaño et al.|Unknown|2024Cited by 0