Rubinstein-Taybi syndrome: MedlinePlus Genetics

Rubinstein-Taybi syndrome is a condition characterized by short stature, moderate to severe intellectual disability, distinctive facial features, and broad thumbs and first toes . Explore symptoms, inheritance, genetics of this condition.

Pediatric on Squares on X: Rubinstein Taybi Syndrome #Pediatric

Fetal phenotype of Rubinstein‐Taybi syndrome caused by CREBBP

Frontiers Behavioral and neuropsychiatric challenges across the

Identification of 22q11.2 deletion in a patient with schizophrenia

Empirical Literature on Rubinstein-Taybi Syndrome (RTS) Meeting

Frontiers Behavioral and neuropsychiatric challenges across the

Molecular studies in 10 cases of Rubinstein-Taybi syndrome

Rubinstein-Taybi Syndrome Awareness

IJMS, Free Full-Text

Genes, Free Full-Text

Chromosome 16: MedlinePlus Genetics

Canal Dehiscense