Library

Kelley EF, Cross TJ, Snyder EM, McDonald CM, Hoffman EP, Bello L. Influence of beta2 adrenergic receptor genotype on risk…

Thangarajh M, Hendriksen J, McDermott MP, Martens W, Hart KA, Griggs RC. Relationships between DMD mutations and neurodevelopment in dystrophinopathy.…

Annexstad EJ, Fagerheim T, Holm I, Rasmussen M. Molecular and Clinical Characteristics of a National Cohort of Paediatric Duchenne Muscular…

Yang Y, He P, Li DZ. Germline mosaicism in a DMD family: incidental identification in prenatal diagnosis. Journal of obstetrics…

Toksoy G, Durmus H, Aghayev A, et al. Mutation spectrum of 260 dystrophinopathy patients from Turkey and important highlights for…

Kong X, Zhong X, Liu L, Cui S, Yang Y, Kong L. Genetic analysis of 1051 Chinese families with Duchenne/Becker…

Yang YM, Yan K, Liu B, et al. Comprehensive genetic diagnosis of patients with Duchenne/Becker muscular dystrophy (DMD/BMD) and pathogenicity…

Aartsma-Rus A, den Dunnen JT. Phenotype predictions for exon deletions/duplications: A user guide for professionals and clinicians using Becker and…

Park J, Jang W, Han JY. Differing disease phenotypes of Duchenne muscular dystrophy and Moyamoya disease in female siblings of…

Polavarapu K, Preethish-Kumar V, Sekar D, et al. Mutation pattern in 606 Duchenne muscular dystrophy children with a comparison between…