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Cryptic FMR1 mosaic deletion in a phenotypically normal mother of a boy with fragile X syndrome: case report

Shiyu Luo, Wen Huang, Qiuping Xia, Yan Xia, Qian Du, Lingqian Wu* and Ranhui Duan*

BMC Medical Genetics 2014, 15:125  doi:10.1186/s12881-014-0125-2

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