Publication | Open Access
Exome-wide Association Study Identifies GREB1L Mutations in Congenital Kidney Malformations
105
Citations
62
References
2017
Year
Developmental BiologyMendelian DisorderGenetic DisorderGeneticsInherited Metabolic DiseaseGenetic EpidemiologyMolecular GeneticsCongenital Kidney MalformationsGenomicsDisease Gene IdentificationMedicineClinical Genetics
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