Rubinstein-Taybi syndrome with agenesis of corpus callosum. - Abstract - Europe PMC
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Last updated 26 abril 2025


File:Rubinstein-Taybi Syndrome1.jpg - Wikipedia

Congenital basis of posterior fossa anomalies. - Abstract - Europe PMC

Rubinstein-Taybi syndrome with agenesis of corpus callosum. - Abstract - Europe PMC

Rubinstein–Taybi syndrome: New neuroradiological and neuropsychiatric insights from a multidisciplinary approach - Ajmone - 2018 - American Journal of Medical Genetics Part B: Neuropsychiatric Genetics - Wiley Online Library

Clinical exome sequencing identifies novel CREBBP variants in 18 Chinese Rubinstein–Taybi Syndrome kids with high frequency of polydactyly - Yu - 2019 - Molecular Genetics & Genomic Medicine - Wiley Online Library

IJMS, Free Full-Text

Congenital basis of posterior fossa anomalies. - Abstract - Europe PMC

Emss 68524

From neural development to cognition: unexpected roles for chromatin. - Abstract - Europe PMC

Emss 68524

Bi-allelic TTC5 variants cause delayed developmental milestones and intellectual disability. - Abstract - Europe PMC

Identification of 22q11.2 deletion in a patient with schizophrenia and clinically diagnosed Rubinstein–Taybi syndrome - Nagai - 2022 - Psychiatry and Clinical Neurosciences Reports - Wiley Online Library

Congenital basis of posterior fossa anomalies. - Abstract - Europe PMC
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