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
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Rubinstein–Taybi syndrome in diverse populations - Tekendo
Clinical, genetic and imaging findings identify new causes for
Characterization of 14 novel deletions underlying Rubinstein–Taybi
Characterization of 14 novel deletions underlying Rubinstein–Taybi
Rubinstein–Taybi syndrome associated with Chiari type I
PDF) Rubinstein-Taybi syndrome: Clinical features, genetic basis
A novel CREBBP mutation and its phenotype in a case of Rubinstein
Rubinstein–Taybi syndrome - Wikipedia
Mosaic CREBBP mutation causes overlapping clinical features of
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Rubinstein–Taybi syndrome: clinical and molecular overview
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