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KANSL1;jsessionid=595BAA89C4BBB6CBABB102C00830CE7F
(gene)
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Thymus gland
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Koolen-de Vries syndrome in the first adulthood patient of Southern India ancestry.
Integrating genome-wide association study and expression quantitative trait loci data identifies mul…
Mutations in KANSL1 cause the 17q21.31 microdeletion syndrome phenotype.
Family based genome-wide copy number scan identifies complex rearrangements at 17q21.31 in dyslexics…
Clinical and molecular characterization of 17q21.31 microdeletion syndrome in 14 French patients wit…
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There were no clinical trials for KANSL1;jsessionid=595BAA89C4BBB6CBABB102C00830CE7F
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