Rubinstein–Taybi syndrome associated with Chiari type I malformation caused by a large 16p13.3 microdeletion: A contiguous gene syndrome? - Wójcik - 2010 - American Journal of Medical Genetics Part A - Wiley Online Library

PDF) Clinical, genetic and imaging findings identify new causes

Fetal phenotype of Rubinstein‐Taybi syndrome caused by CREBBP

Clinical, genetic and imaging findings identify new causes for

Rubinstein-Taybi Syndrome: spectrum of CREBBP mutations in Italian

Characterization of 14 novel deletions underlying Rubinstein–Taybi

PDF) The Social Security Administration's Compassionate Allowances

Dominant variants in the splicing factor PUF60 cause a

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

Rubinstein-Taybi syndrome: MedlinePlus Genetics

High frequency of copy number imbalances in Rubinstein–Taybi

Rubinstein-Taybi syndrome with scoliosis treated with single-stage

PDF) The Social Security Administration's Compassionate Allowances

Rubinstein–Taybi syndrome: New neuroradiological and

Frontiers Genetic Diagnosis of Rubinstein–Taybi Syndrome With