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BMC Pediatrics|December 29, 2022
Poland-Möbius syndrome: a case report implicating a novel mutation of the PLXND1 gene and literature reviewGraeme E Glass, Shiyas Mohammedali, Bran Sivakumar, et al.Journal of Neuromuscular Diseases|July 25, 2018
Impacts for Children Living with Genetic Muscle Disorders and their Parents - Findings from a Population-Based StudyKelly M Jones, Gina O'Grady, Miriam J Rodrigues, et al.The Annals of Thoracic Surgery|July 1, 1987
Maximal oxygenation of dilute blood cardioplegic solutionW G Hendren, D D O'Keefe, G A Geffin, et al.Cancer Letters|October 26, 1999
Serum homocysteine levels in postmenopausal breast cancer patients treated with tamoxifenR R Love, G Anker, Y Yang, et al.Biochemical and Biophysical Research Communications|August 21, 2001
Dystrophin in adult zebrafish muscleS P Chambers, A Dodd, R Overall, et al.Archives of Internal Medicine|October 1, 1985
Massive skeletal muscle invasion by lymphomaJ L Grem, A J Neville, S C Smith, et al.Molecular Genetics & Genomic Medicine|April 12, 2020
Haploinsufficiency of the FOXA2 associated with a complex clinical phenotypeIdris Mohammed, Sara Al-Khawaga, David Bohanna, et al.Applied and Environmental Microbiology|October 1, 1990
celB, a gene coding for a bifunctional cellulase from the extreme thermophile "Caldocellum saccharolyticum"D J Saul, L C Williams, R A Grayling, et al.American Journal of Human Genetics|July 1, 1993
Monoclonal antibodies against the muscle-specific N-terminus of dystrophin: characterization of dystrophin in a muscular dystrophy patient with a frameshift deletion of exons 3-7T T Le, T M Nguyen, D R Love, et al.American Journal of Medical Genetics|January 1, 1991
Linkage analysis in families with autosomal recessive limb-girdle muscular dystrophy (LGMD) and 6q probes flanking the dystrophin-related sequenceM R Passos-Bueno, J Terwilliger, J Ott, et al.Pageof 51