Associated Papers
Uncovering the true features of dystrophin gene rearrangement and improving the molecular diagnosis of Duchenne and Becker muscular dystrophies.
Ling C et al.
Iscience, 2023
38047063 (PubMed )
Supplement: mmc3.xlsx › Sheet1
Exonic rearrangements in DMD in Chinese Han individuals affected with Duchenne and Becker muscular dystrophies.
Ling C et al.
Human Mutation, 2020
31705731 (PubMed )
Supplement: HUMU-41-668-s002.xlsx › Sheet1
Application of Next-Generation Sequencing for Genetic Diagnosis in Neonatal Intensive Care Units: Results of a Multicenter Study in China.
Zhu T et al.
Frontiers in Genetics, 2020
A new approach to gene diagnosis of Duchenne/Becker muscular dystrophy--amplified fragment length polymorphisms.
Xu S et al.
Chinese Medical Sciences Journal = Chung-kuo I Hsueh K'o Hsueh Tsa Chih, 1994
Microlesions and polymorphisms in the Duchenne/Becker muscular dystrophy gene.
Rininsland F et al.
Human Genetics, 1994
[Genomic structure and DNA diagnosis of hereditary monogenic diseases in the Volga-Ural region].
Khidiiatova IM et al.
Molekuliarnaia Biologiia, 0
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