Heterozygous rare variants in NR2F2 cause a recognizable multiple congenital anomaly syndrome with developmental delays - Concepedia

Concepedia

Publication | Open Access

Heterozygous rare variants in NR2F2 cause a recognizable multiple congenital anomaly syndrome with developmental delays

DOI Full Paper Access

23

Citations

33

References

2023

Year

Mythily Ganapathi, Leticia S. Matsuoka, Michael March, Dong Li, Elly Brokamp, Sara Benito‐Sanz, Susan M. White, Katherine Lachlan, Priyanka Ahimaz, Anshuman Sewda,

European Journal of Human Genetics

Developmental AnomalyDevelopmental BiologyMendelian DisorderGenetic DisorderGeneticsInherited Metabolic DiseaseDevelopmental DelaysMolecular GeneticsAbnormal DevelopmentMedicineClinical GeneticsHeterozygous Rare Variants

References

	Year	Citations

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