SÍNDROME DE RUBINSTEIN-TAYBI - CANAL INFANTIL

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First case report of inherited Rubinstein-Taybi syndrome associated with a novel EP300 variant, BMC Medical Genetics

Síndrome de Rubinstein-Taybi – FEMEXER

SciELO - Brasil - Síndrome de Rubinstein-Taybi: anomalias físicas, manifestações clínicas e avaliação auditiva Síndrome de Rubinstein-Taybi: anomalias físicas, manifestações clínicas e avaliação auditiva

Lucía, la niña del 'síndrome de los pulgares anchos' y la sonrisa contagiosa

PDF) Genetic heterogeneity in Rubinstein-Taybi syndrome: Delineation of the phenotype of the first patients carrying mutations in EP300

Mosaic CREBBP mutation causes overlapping clinical features of Rubinstein–Taybi and Filippi syndromes

Rubinstein–Taybi syndrome in diverse populations - Tekendo‐Ngongang - 2020 - American Journal of Medical Genetics Part A - Wiley Online Library

Rubinstein-Taybi syndrome: clinical features, genetic basis, diagnosis, and management, Italian Journal of Pediatrics

Molecular studies in 10 cases of Rubinstein-Taybi syndrome