Publication | Open Access
FOXG1 syndrome: genotype–phenotype association in 83 patients with FOXG1 variants
108
Citations
32
References
2017
Year
Genetic DisorderGeneticsGenetic EpidemiologyClinical GeneticsPathologyMolecular GeneticsDisease Gene IdentificationPublic HealthMedicineMonogenic DisordersFoxg1 Syndrome
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