NRF1 Association with AUTS2-Polycomb Mediates Specific Gene Activation in the Brain

Rubinstein–Taybi syndrome - Wikipedia

Figure 2. [Broad terminal phalanges (A) and broad, radially deviated thumbs (B)]. - GeneReviews® - NCBI Bookshelf

Rubinstein Taybi syndrome causes, symptoms, diagnosis, treatment & prognosis

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Cureus, Whole-Exome Sequencing Identified a Novel DYRK1A Variant in a Patient With Intellectual Developmental Disorder, Autosomal Dominant 7

Floating-Harbor syndrome: MedlinePlus Genetics

PDF) Rubinstein-Taybi syndrome in diverse populations

Müllerian Agenesis in a patient with Rubinstein-Taybi Syndrome: A Case Series and Review of the Overlapping Developmental Biologic Pathways - Journal of Pediatric and Adolescent Gynecology

A novel CREBBP mutation and its phenotype in a case of Rubinstein

(PDF) Identification of de novo EP300 and PLAU variants in a patient with Rubinstein–Taybi syndrome-related arterial vasculopathy and skeletal anomaly