Prenatal diagnosis for a Chinese family with a de novo DMD gene mutation

Author:

Li Tao,Zhang Zhao-jing,Ma Xin,Lv Xue,Xiao Hai,Guo Qian-nan,Liu Hong-yan,Wang Hong-dan,Wu Dong,Lou Gui-yu,Wang Xin,Zhang Chao-yang,Liao Shi-xiu

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

General Medicine

Reference25 articles.

1. Non-invasive prenatal diagnosis of Duchenne and Becker muscular dystrophies by relative haplotype dosage;Parks;Prenat Diagn,2016

2. Non-invasive biomarkers for Duchenne muscular dystrophy and carrier detection;Anaya-Segura;Molecules,2015

3. Predictive value of MLPA combined with STR gene Linkage analysis in prenatal diagnosis of DMD;Li;Chin J Met Genet,2013

4. Genetic diagnosis and prenatal diagnosis for a family without deletions and duplications on Dystrophin gene exon;Li;Chin J Met Genet,2015

5. Complete cloning of the Duchenne muscular dystrophy (DMD) cDNA and preliminary genomic organization of the DMD gene in normal and affected individuals;Koenig;Cell,1987

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