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Autor:
Stephanie A Felker, James MJ Lawlor, Susan M Hiatt, Michelle L Thompson, Donald R Latner, Candice R Finnila, Kevin M Bowling, Zachary T Bonnstetter, Katherine E Bonini, Nicole R Kelly, Whitley V Kelley, Anna CE Hurst, Melissa A Kelly, Ghunwa Nakouzi, Laura G Hendon, E Martina Bebin, Eimear E Kenny, Gregory M Cooper
PurposeNeurodevelopmental disorders (NDDs) often result from rare genetic variation, but genomic testing yield for NDDs remains around 50%, suggesting some clinically relevant rare variants may be missed by standard analyses. Here we analyze “poiso
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1d216d5994ea7884fe8a6e070dedbfec
https://doi.org/10.1101/2023.01.12.523654
https://doi.org/10.1101/2023.01.12.523654