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SFARI

Tag: copy number variation

March 06, 2023

A new approach to analyzing genomic association data finds convergence of both rare and common genetic influences on autism at chromosome 16p By Azra Jaferi
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August 18, 2022

Clinical trial of arbaclofen for 16p11.2 deletion has launched By Rachel Jurd
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March 15, 2022

Copy number variation and pathogenic variant analyses of SPARK exomes

January 28, 2022

Simons Searchlight: December 2021 data release
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December 20, 2021

Simons Searchlight to host conference on CSNK2A1, HIVEP2, MED13L and SETBP1 genes
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December 13, 2021

New iPSC lines from Simons Searchlight participants are now available
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