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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PDF) Rubinstein-Taybi syndrome: Clinical features, genetic basis
A novel CREBBP mutation and its phenotype in a case of Rubinstein
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PDF) Rubinstein-Taybi syndrome: Clinical features, genetic basis
Rubinstein–Taybi syndrome: New neuroradiological and
Microdeletions and mutations of CREBBP (CBP) gene can cause
Further delineation of an entity caused by CREBBP and EP300
Molecular studies in 10 cases of Rubinstein-Taybi syndrome
Rubinstein–Taybi syndrome - Wikipedia
EP300‐related Rubinstein–Taybi syndrome: Highlighted rare
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