Autism Spectrum Disorder

Rubinstein–Taybi syndrome - Wikipedia

Rubinstein-Taybi Syndrome 1

Facial features of Rubinstein-Taybi syndrome

Genetic Heterogeneity in Rubinstein-Taybi Syndrome: Mutations in

a,b: Patient A at 3 weeks; c,d: Patient B at 6 weeks, note the

Rubinstein-Taybi syndrome 2 with cerebellar abnormality and neural

Rubinstein-Taybi syndrome: Treatments and life expectancy

Thyroid Hypoplasia as a Cause of Congenital Hypothyroidism in

First case of Rubinstein–Taybi syndrome with desquamation associated with a novel mutation in the bromodomain of the CREBBP gene - Wang - 2019 - Clinical and Experimental Dermatology - Wiley Online Library

Mosaic CREBBP mutation causes overlapping clinical features of