Rubinstein-Taybi syndrome (RTS)

Rubinstein–Taybi syndrome - Wikipedia

Anaesthesia Management in a Child with Rubinstein - Taybi Syndrome

Mutations in SRCAP, Encoding SNF2-Related CREBBP Activator Protein, Cause Floating-Harbor Syndrome - ScienceDirect

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

Cornelia de Lange Syndrome - GeneReviews® - NCBI Bookshelf

Floating-Harbor syndrome: MedlinePlus Genetics

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

Somatic and germ‐line mosaicism in Rubinstein–Taybi syndrome - Chiang - 2009 - American Journal of Medical Genetics Part A - Wiley Online Library

Rubinstein-Taybi syndrome with agenesis of corpus callosum. - Abstract - Europe PMC

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