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

Rubinstein-Taybi syndrome with scoliosis treated with single-stage

Rubinstein-Taybi Syndrome: A case report

PDF) Rubinstein-Taybi syndrome: Clinical features, genetic basis

Rubinstein–Taybi syndrome associated with Chiari type I

Duplication 16p13.3 and the CREBBP gene: Confirmation of the

Rubinstein-Taybi syndrome with scoliosis treated with single-stage

Mosaic CREBBP mutation causes overlapping clinical features of

Rubinstein–Taybi syndrome in diverse populations - Tekendo

Rubinstein–Taybi syndrome in diverse populations - Tekendo

Characterization of 14 novel deletions underlying Rubinstein–Taybi