Parental origin of the de novo 22q13 deletions.
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Parental origin of the de novo 22q13 deletions.
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创建时间：
2015-12-02
相关数据集
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Coordinates of Xp11.22 deletions and Xp11.22 genes previously implicated or proposed to be involved in the development of intellectual disability/developmental delay/autism.
Coordinates of Xp11.22 deletions and Xp11.22 genes previously implicated or proposed to be involved in the development of intellectual disability/developmental delay/autism.
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Additional file 8 of A nuclear transport-related gene signature combined with IDH mutation and 1p/19q codeletion better predicts the prognosis of glioma patients
Additional file 8: Supplemental Table 4. The sequences of the primers.
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