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1.
Molecular Genetic Diagnosis For Fetus With Congenital Heart Disease
2.
Clinical And ANO5 Genetic Features In A Chinese Family With Limb Girdle Muscular Dystrophy 2L
3.
The Research Of Phenylalanine Hydroxylase Mutation In Patients With Phenylketonuria
4.
Expression And Significance Of SLC35E2B Gene Variation In Plaque Psoriasis
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