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Case Reports
. 1995 Sep;4(9):1681-4.
doi: 10.1093/hmg/4.9.1681.

Spontaneous deletion in the FMR1 gene in a patient with fragile X syndrome and cherubism

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Case Reports

Spontaneous deletion in the FMR1 gene in a patient with fragile X syndrome and cherubism

F Quan et al. Hum Mol Genet. 1995 Sep.
No abstract available

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