Publication | Closed Access
De novo MECP2 duplications in two females with intellectual disability and unfavorable complete skewed X-inactivation
60
Citations
34
References
2014
Year
Mecp2 DuplicationsMendelian DisorderGenetic DisorderGeneticsFragile X SpectrumPathologyMolecular GeneticsDisease Gene IdentificationMedicineFragile X PremutationDevelopmental Delay
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