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- W2354339966 abstract "Objective:To determine the genetic type of a fetus with Duchenne muscular dystrophy (DMD) pedigree,and to search the experimental method for prenatal gene diagnosis of DMD. Methods:The DNA of the fetus and other family members were obtained respectively by TRIzol and Promega blood extracted kit from the amniotic fluid and peripheral blood. Six pairs of fluorescent primers near the Xp21.1 were chosen for PCR and linkage analysis,by which the risk X chromosome was determined. Through the multiple PCR assay with the primers of DMD50 and SRY,the gender of the fetus was determined. Results:The fetus was female and normal,and did not carry the risk X chromosome. Conclusion:This method can not only enlarge the range of gene examination,but also finish the test of non-deletion or/and deletion DMD risk fetus in one step. It makes the result much more reliable." @default.
- W2354339966 created "2016-06-24" @default.
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- W2354339966 date "2009-01-01" @default.
- W2354339966 modified "2023-09-23" @default.
- W2354339966 title "Prenatal Gene Diagnosis for the Duchenne Muscular Dystrophy Risk Fetus by Molecule Markers" @default.
- W2354339966 hasPublicationYear "2009" @default.
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