Rubinstein-Taybi syndrome with agenesis of corpus callosum. - Abstract - Europe PMC
Por um escritor misterioso
Last updated 25 março 2025


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
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