Robinow Syndrome: Most Up-to-Date Encyclopedia, News & Reviews

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Rubinstein-Taybi Syndrome 1

A mosaic maternal splice donor mutation in the EHMT1 gene leads to aberrant transcripts and to Kleefstra syndrome in the offspring

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

Silver Russell Syndrome: Most Up-to-Date Encyclopedia, News & Reviews

Legius Syndrome - an overview

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

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

Frontiers Behavioral and neuropsychiatric challenges across the lifespan in individuals with Rubinstein-Taybi syndrome

Rubinstein-Taybi syndrome with agenesis of corpus callosum