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

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Duplications of the critical Rubinstein–Taybi deletion region on

PDF) Clinical, genetic and imaging findings identify new causes

Mosaic CREBBP mutation causes overlapping clinical features of

Rubinstein–Taybi syndrome in diverse populations - Tekendo

Molecular analysis of the CBP gene in 60 patients with Rubinstein

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Novel cAMP binding protein-BP (CREBBP) mutation in a girl with

Rubinstein–Taybi syndrome: New neuroradiological and

PDF) The Social Security Administration's Compassionate Allowances