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Methods in Molecular Biology (Clifton, N.J.)|November 9, 2016
Analyzing Copy Number Variation Using Pulsed-Field Gel Electrophoresis: Providing a Genetic Diagnosis for FSHD1Richard J L F LemmersMuscle & Nerve|December 7, 2007
Atypical facet of Möbius syndrome: association with facioscapulohumeral muscular dystrophyHanna K Kolski, Norma J Leonard, Richard J L F Lemmers, et al.Communications Biology|June 5, 2026
The emergence and diversification of the DUX gene family across placental mammalsAlberto Budillon, Richard J L F Lemmers, Stephen J Tapscott, et al.Pediatric Nephrology (Berlin, Germany)|March 2, 2010
Focal segmental glomerulosclerosis, Coats'-like retinopathy, sensorineural deafness and chromosome 4 duplication: a new associationBen C Reynolds, Richard J L F Lemmers, John Tolmie, et al.Human Molecular Genetics|May 28, 2014
DUX4-induced gene expression is the major molecular signature in FSHD skeletal muscleZizhen Yao, Lauren Snider, Judit Balog, et al.Neuromuscular Disorders : NMD|July 1, 2008
Phenotype of combined Duchenne and facioscapulohumeral muscular dystrophyLawrence Korngut, Victoria M Siu, Shannon L Venance, et al.Neurology|November 13, 2015
Milder phenotype in facioscapulohumeral dystrophy with 7-10 residual D4Z4 repeatsJeffrey M Statland, Colleen M Donlin-Smith, Stephen J Tapscott, et al.Annals of Neurology|June 3, 2004
Somatic mosaicism in FSHD often goes undetectedRichard J L F Lemmers, Michiel J R van der Wielen, Egbert Bakker, et al.Human Genetics|January 13, 2005
Genetic confirmation of facioscapulohumeral muscular dystrophy in a case with complex D4Z4 rearrangmentsBorian T Buzhov, Richard J L F Lemmers, Ivailo Tournev, et al.Nature Genetics|October 2, 2002
Facioscapulohumeral muscular dystrophy is uniquely associated with one of the two variants of the 4q subtelomereRichard J L F Lemmers, Peggy de Kievit, Lodewijk Sandkuijl, et al.Pageof 7