Publication | Open Access
Prospective cohort study for identification of underlying genetic causes in neonatal encephalopathy using whole-exome sequencing
51
Citations
34
References
2017
Year
Genetic DisorderWhole-exome SequencingGeneticsGenetic EpidemiologyPediatricsNeurologyUnderlying Genetic CausesDisease Gene IdentificationMedicineSequencingProspective Cohort Study
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