Point mutation screening in exon 1 to 10 of DMD and optimization of Multiplex Ligation Probe-dependent Amplification (MLPA) in a DMD cohort /

مواد مشابهة

• The role of lipid peroxidation in the pathogenesis of duchenne muscular dystrophy /
  بواسطة: Jamaludin bin Mohamed
  منشور في: (1984)
• Mutation and heterozygote carrier detection in duchenne muscular dystrophy in Malaysia
  بواسطة: Mohd. Fariddudin Mohd. Yusof
  منشور في: (2002)
• Molecular detection of normal and expanded CTG alleles and microRNA expression aberration in Myotonic Dystrophy type 1 /
  بواسطة: Ambrose Michael, Kathlin Kaminiy
  منشور في: (2015)
• Prevalence of musculoskeletal symptoms and associated risk factors among workers in the printing industry
  بواسطة: Foong , May Chi
  منشور في: (2012)
• Muscle mass, clinical outcome and protein delivery in critically ill patients /
  بواسطة: Lee, Zheng Yii
  منشور في: (2022)