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10.3389/fped.2021.713458

Case Report: Progressive Cholestasis: Severe Phenotype of MEGDEL Syndrome With SATB2-Associated Syndrome


10.3389/fgene.2021.692087

Case Report: SATB2-Associated Syndrome Overlapping With Clinical Mitochondrial Disease Presentation: Report of Two Cases


10.1111/scd.12340

SATB2‐associated syndrome (SAS) and associated dental findings



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10.3389/fnmol.2019.00033

Loss of Satb2 in the Cortex and Hippocampus Leads to Abnormal Behaviors in Mice


10.3389/fgene.2019.00630

Paternal Low-Level Mosaicism-Caused SATB2-Associated Syndrome


10.1097/MCD.0000000000000293

SATB2-associated syndrome: first report of a gonadal and somatic mosaicism for an intragenic copy number variation.


10.3760/CMA.J.ISSN.1006-7876.2019.12.010

Special AT-rich binding protein 2-associated syndrome: a case report and literature review


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