Molecular studies in 10 cases of Rubinstein-Taybi syndrome
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Clinical photos of the patients. (a) Case 1: Dysmorphic facial features
A case of bilateral elbow dislocation in a patient with Rubinstein-Taybi syndrome - JSES International
IJMS, Free Full-Text
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Frontiers Genetic Diagnosis of Rubinstein–Taybi Syndrome With Multiplex Ligation-Dependent Probe Amplification (MLPA) and Whole-Exome Sequencing (WES): Case Series With a Novel CREBBP Variant
Epigenetic mechanisms of Rubinstein-Taybi syndrome. - Abstract - Europe PMC
Rubinstein-Taybi syndrome in a Saudi boy with distinct features and variants in both the CREBBP and EP300 genes: a case report, BMC Medical Genetics
Molecular analysis of the CBP gene in 60 patients with Rubinstein-Taybi syndrome
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Rubinstein-Taybi Syndrome
Rubinstein-Taybi syndrome with scoliosis – topic of research paper in Clinical medicine. Download scholarly article PDF and read for free on CyberLeninka open science hub.
CBP-HSF2 structural and functional interplay in Rubinstein-Taybi neurodevelopmental disorder
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