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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Frontiers Case Report: Low-Level Maternal Mosaicism of a Novel
A novel CREBBP mutation and its phenotype in a case of Rubinstein
Rubinstein-Taybi syndrome with scoliosis treated with single-stage
Molecular analysis of the CBP gene in 60 patients with Rubinstein
Clinical, genetic and imaging findings identify new causes for
PDF) Rubinstein-Taybi syndrome: Clinical features, genetic basis
Clinical, genetic and imaging findings identify new causes for
Clinical, genetic and imaging findings identify new causes for
Rubinstein–Taybi syndrome: clinical and molecular overview
Genes, Free Full-Text
Mosaic CREBBP mutation causes overlapping clinical features of
Molecular studies in 10 cases of Rubinstein-Taybi syndrome
Rubinstein-Taybi syndrome in a Saudi boy with distinct features
Rubinstein–Taybi syndrome associated with Chiari type I
