4 Newborn with Rubinstein-Taybi syndrome showing microcephaly

Characterization of 14 novel deletions underlying Rubinstein–Taybi syndrome: an update of the CREBBP deletion repertoire

4 Newborn with Rubinstein-Taybi syndrome showing microcephaly, frontal

Microcephaly - UF Health

New insights into genetic variant spectrum and genotype–phenotype correlations of Rubinstein‐Taybi syndrome in 39 CREBBP‐positive patients - Pérez‐Grijalba - 2019 - Molecular Genetics & Genomic Medicine - Wiley Online Library

Frontiers Case report: A preterm infant with rubinstein-taybi syndrome and Marmorata telangiectatica harboring a frameshift mutation in the CREBBP gene

Ocular features in Rubinstein-Taybi syndrome: investigation of 24 patients and review of the literature

Clinical exome sequencing identifies novel CREBBP variants in 18 Chinese Rubinstein–Taybi Syndrome kids with high frequency of polydactyly - Yu - 2019 - Molecular Genetics & Genomic Medicine - Wiley Online Library

An approach to a chil with microcephaly

JaypeeDigital

Rubinstein-Taybi Syndrome: A Complete Overview — DermNet

Case report: a Chinese girl like atypical Rubinstein–Taybi syndrome caused by a novel heterozygous mutation of the EP300 gene, BMC Medical Genomics