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

Rubinstein–Taybi syndrome - Wikipedia

Severe persistent pulmonary hypertension in a neonate with

Floating-Harbor syndrome: MedlinePlus Genetics

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

Expanding the phenotype associated to KMT2A variants: overlapping clinical signs between Wiedemann–Steiner and Rubinstein–Taybi syndromes

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

Approach to inherited hypertrichosis: A brief review - Indian Journal of Dermatology, Venereology and Leprology

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

(PDF) Identification of de novo EP300 and PLAU variants in a