Table S1 - High Frequency of Copy Number Variations and Sequence Variants at CYP21A2 Locus: Implication for the Genetic Diagnosis of 21-Hydroxylase Deficiency
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https://figshare.com/articles/dataset/High_Frequency_of_Copy_Number_Variations_and_Sequence_Variants_at_CYP21A2_Locus_Implication_for_the_Genetic_Diagnosis_of_21_Hydroxylase_Deficiency/150637
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Sequences of primers. (0.03 MB DOC)
引物序列。（0.03 MB，DOC格式）
创建时间：
2015-12-02
