Genomic study of severe fetal anomalies and discovery of GREB1L mutations in renal agenesis - Concepedia

Concepedia

Publication | Open Access

Genomic study of severe fetal anomalies and discovery of GREB1L mutations in renal agenesis

DOI Full Paper Access

82

Citations

37

References

2017

Year

Sarah Boissel, Catherine Fallet‐Bianco, David Chitayat, Valérie Kremer, Christina Nassif, Françoise Rypens, Marie‐Ange Delrue, Dorothée Dal Soglio, Luc L. Oligny, Natalie Patey,

Genetics in Medicine

Developmental AnomalySevere Fetal AnomaliesDevelopmental BiologyGreb1l MutationsMendelian DisorderGenetic DisorderGeneticsInherited Metabolic DiseaseRenal AgenesisMolecular GeneticsDisease Gene IdentificationGenomicsMedicineClinical Genetics

References

	Year	Citations

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