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

Reprogramming of the epigenome in neurodevelopmental disorders. - Abstract - Europe PMC

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

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

Reprogramming of the epigenome in neurodevelopmental disorders. - Abstract - Europe PMC

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

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

Genes, Free Full-Text

Rubinstein-Taybi syndrome: Multisystem involvement and its clinical

Haploinsufficiency of the Sin3/HDAC corepressor complex member SIN3B causes a syndromic intellectual disability/autism spectrum disorder. - Abstract - Europe PMC

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

Haploinsufficiency of the Sin3/HDAC corepressor complex member SIN3B causes a syndromic intellectual disability/autism spectrum disorder. - Abstract - Europe PMC

A case with Rubinstein-Taybi syndrome: A novel frameshift mutation in the CREBBP gene.

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

Rubinstein–Taybi syndrome - Wikipedia