4.3 Letter

Phenotype of ASDs Associated With 4p16 Risk Locus and Novel Genome-Wide Associations of ASD Patients in the Finnish Population

Journal

CIRCULATION-GENOMIC AND PRECISION MEDICINE
Volume 16, Issue 5, Pages 486-489

Publisher

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1161/CIRCGEN.123.004070

Keywords

genetic loci; genome; heart defects, congenital; heart septal defect, atrial; mutation

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