De novo variants in FRYL are associated with developmental delay, intellectual disability, and dysmorphic features
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Published:2024-04
Issue:4
Volume:111
Page:742-760
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ISSN:0002-9297
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Container-title:The American Journal of Human Genetics
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language:en
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Short-container-title:The American Journal of Human Genetics
Author:
Pan Xueyang, Tao Alice M., Lu Shenzhao, Ma Mengqi, Hannan Shabab B., Slaugh Rachel, Drewes Williams Sarah, O'Grady Lauren, Kanca Oguz, Person Richard, Carter Melissa T., Platzer Konrad, Schnabel Franziska, Abou Jamra Rami, Roberts Amy E., Newburger Jane W., Revah-Politi Anya, Granadillo Jorge L., Stegmann Alexander P.A., Sinnema Margje, Accogli Andrea, Salpietro Vincenzo, Capra Valeria, Ghaloul-Gonzalez Lina, Brueckner Martina, Simon Marleen E.H., Sweetser David A., Glinton Kevin E., Kirk Susan E., Burrage Lindsay C., Heaney Jason D., Kim Seon-Young, Lanza Denise G., Liu Zhandong, Mao Dongxue, Milosavljevic Aleksander, Nagamani Sandesh C.S., Posey Jennifer E., Ramamurthy Uma, Ramanathan Vivek, Rogers Jeffrey, Rosenfeld Jill A., Roth Matthew, Zahedi Darshoori Ramin, Wangler Michael F., Yamamoto Shinya, Chung Wendy K., Bellen Hugo J.ORCID
Funder
NIH ORIP Huffington Foundation National Heart Lung and Blood Institute National Center for Advancing Translational Sciences Eunice Kennedy Shriver National Institute of Child Health and Human Development
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