Human Genome Epidemiology Literature Finder
Records 1 - 3 (of 3 Records) |
Query Trace: Syndrome and DMD[original query] |
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Neurodevelopmental, emotional, and behavioural problems in Duchenne muscular dystrophy in relation to underlying dystrophin gene mutations. Developmental medicine and child neurology 2015 Sep . Ricotti Valeria, Mandy William Pl, Scoto Mariacristina, Pane Marika, Deconinck Nicolas, Messina Sonia, Mercuri Eugenio, Skuse David H, Muntoni Frances |
Whole genome sequencing reveals a 7 base-pair deletion in DMD exon 42 in a dog with muscular dystrophy. Mammalian genome : official journal of the International Mammalian Genome Society 2016 12 28 (3-4): 106-113. Nghiem Peter P, Bello Luca, Balog-Alvarez Cindy, López Sara Mata, Bettis Amanda, Barnett Heather, Hernandez Briana, Schatzberg Scott J, Piercy Richard J, Kornegay Joe |
Clinical and genetic characteristics of Chinese Duchenne/Becker muscular dystrophy patients with small mutations. Frontiers in neuroscience 2022 11 16 992546. Gan Siyi, Liu Shulei, Yang Haiyan, Wu Liw |
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