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American Journal of Human Genetics|May 14, 2019

Heterozygous Variants in KMT2E Cause a Spectrum of Neurodevelopmental Disorders and EpilepsyAnne H O'Donnell-Luria, Lynn S Pais, Víctor Faundes, et al.

The Journal of Clinical Investigation|November 14, 2023

Spliceosome malfunction causes neurodevelopmental disorders with overlapping featuresDong Li, Qin Wang, Allan Bayat, et al.

Nature Genetics|October 22, 2025

Pathogenic UNC13A variants cause a neurodevelopmental syndrome by impairing synaptic functionReza Asadollahi, Aisha Ahmad, Paranchai Boonsawat, et al.

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Search research articles

Showing results (741-750 of 743) with videos related to

Sort By:

Pageof 75

You have reached the last page of results.This site can display upto 743 results.

American Journal of Human Genetics|May 14, 2019

Heterozygous Variants in KMT2E Cause a Spectrum of Neurodevelopmental Disorders and EpilepsyAnne H O'Donnell-Luria, Lynn S Pais, Víctor Faundes, et al.

The Journal of Clinical Investigation|November 14, 2023

Spliceosome malfunction causes neurodevelopmental disorders with overlapping featuresDong Li, Qin Wang, Allan Bayat, et al.

Nature Genetics|October 22, 2025

Pathogenic UNC13A variants cause a neurodevelopmental syndrome by impairing synaptic functionReza Asadollahi, Aisha Ahmad, Paranchai Boonsawat, et al.

Pageof 75