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Fig. 2 | Molecular Cytogenetics

Fig. 2

From: A prenatal diagnosis and genetics study of five pedigrees in the Chinese population with Xp22.31 microduplication

Fig. 2

A comparison of the breakpoints of the five pedigrees. Uppermost is a schematic representation of the X chromosome was shown. The red box represents Xp22.31’s genomic location, which has been magnified below. Below, the colour bars represent OMIM genes with the gene’s names below. Beneath the genomic location bars, our pedigrees are represented with gray bars representing the sizes of the duplications

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