Rubinstein-Taybi syndrome - wikidoc

Congenital glaucoma as a presenting feature of Rubinstein-Taybi

Rubinstein-Taybi Syndrome 2 disease: Malacards - Research Articles, Drugs, Genes, Clinical Trials

PDF) Rubinstein-Taybi syndrome medical guidelines

OMIM diseases as a function of associated HPO phenotypes. Data include

Microdeletions and mutations of CREBBP (CBP) gene can cause

Main clinical findings of the 16 Brazilian patients with

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

Rubinstein‐Taybi syndrome in Chinese population with four novel mutations - Yu - 2021 - American Journal of Medical Genetics Part A - Wiley Online Library

High frequency of copy number imbalances in Rubinstein–Taybi

A novel CREBBP mutation and its phenotype in a case of Rubinstein