Leon, Eyby
Children's National
2 papers on CoChatORCID 0000-0002-1852-2849
Most cited papers
- Verified
TFE3‐associated neurodevelopmental disorder: A distinct recognizable syndrome
Diaz, J., Berger, S., & Leon, E. (2020) · American Journal of Medical Genetics Part A
Genomics and Rare DiseasesGenetics and Neurodevelopmental Disorders
Cited by 14
- Verified
ALDH1A2‐related disorder: A new genetic syndrome due to alteration of the retinoic acid pathway
Leon, E., Nde, C., Ray, R. S., Preciado, D., & Zohn, I. E. (2023) · American Journal of Medical Genetics Part A
Congenital limb and hand anomaliesGenomics and Rare Diseases
Cited by 13
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