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1 McKenna A, "The Genome Analysis Toolkit : a MapReduce framework for analyzing next-generation DNA sequencing data" 20 : 1297-1303, 2010
2 Pagliaroli L, "The Evolutionary Conserved SWI/SNF Subunits ARID1A and ARID1B Are Key Modulators of Pluripotency and Cell-Fate Determination" 9 : 643361-, 2021
3 Jayaprakash S, "The ATPase BRG1/SMARCA4 is a protein interaction platform that recruits BAF subunits and the transcriptional repressor REST/NRSF in neural progenitor cells" 461 : 171-182, 2019
4 van der Sluijs PJ, "The ARID1B spectrum in 143 patients : from nonsyndromic intellectual disability to Coffin-Siris syndrome" 21 : 1295-1307, 2019
5 Miraldi Utz V, "Systemic and ocular manifestations of a patient with mosaic ARID1A-associated Coffin-Siris syndrome and review of select mosaic conditions with ophthalmic manifestations" 184 : 644-655, 2020
6 Richards S, "Standards and guidelines for the interpretation of sequence variants : a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology" 17 : 405-424, 2015
7 Stanton BZ, "Smarca4 ATPase mutations disrupt direct eviction of PRC1 from chromatin" 49 : 282-288, 2017
8 Toto PC, "SWI/SNF-directed stem cell lineage specification : dynamic composition regulates specific stages of skeletal myogenesis" 73 : 3887-3896, 2016
9 Zarate YA, "SMARCE1, a rare cause of Coffin-Siris Syndrome : Clinical description of three additional cases" A170 : 1967-1973, 2016
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