Growth charts for individuals with Rubinstein–Taybi syndrome

IJMS, Free Full-Text

Analysis of mutations within the intron20 splice donor site of CREBBP in patients with and without classical RSTS

First case report of inherited Rubinstein-Taybi syndrome associated with a novel EP300 variant – topic of research paper in Clinical medicine. Download scholarly article PDF and read for free on CyberLeninka open

PDF) Rubinstein-Taybi 2 associated to novel EP300 mutations: Deepening the clinical and genetic spectrum

OMIM diseases as a function of associated HPO phenotypes. Data include

About - DECIPHER v11.23

High frequency of copy number imbalances in Rubinstein–Taybi

Rubinstein‐Taybi syndrome in Chinese population with four novel

Genetic heterogeneity in Rubinstein–Taybi syndrome: delineation of

Expanding the phenotype associated to KMT2A variants: overlapping