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- W4283163015 abstract "Here we report a case of a 16q24.3 microdeletion KBG syndrome (KBGS) in a fetus. The absence of a well-defined phenotype poses a challenge for genetic diagnosis. This report demonstrated that the high-risk chromosome 21 trisomy could be the first manifestation of KBGS, as observed in this case." @default.
- W4283163015 created "2022-06-21" @default.
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- W4283163015 date "2022-06-01" @default.
- W4283163015 modified "2023-09-25" @default.
- W4283163015 title "A case of prenatal diagnosis of 16q24.3 microdeletion <scp>KBG</scp> syndrome and review of the literature" @default.
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- W4283163015 doi "https://doi.org/10.1002/ccr3.5958" @default.
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