4 Newborn with Rubinstein-Taybi syndrome showing microcephaly

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Seckel Syndrome: Most Up-to-Date Encyclopedia, News & Reviews

EP300‐related Rubinstein–Taybi syndrome: Highlighted rare phenotypic findings and a genotype–phenotype meta‐analysis of 74 patients - Cohen - 2020 - American Journal of Medical Genetics Part A - Wiley Online Library

Rubinstein-Taybi Syndrome

Genetic heterogeneity in Rubinstein–Taybi syndrome: delineation of the phenotype of the first patients carrying mutations in EP300

Exon deletions of the EP300 and CREBBP genes in two children with Rubinstein –Taybi syndrome detected by aCGH

CREBBP mutations in individuals without Rubinstein–Taybi syndrome phenotype - Menke - 2016 - American Journal of Medical Genetics Part A - Wiley Online Library

4 Newborn with Rubinstein-Taybi syndrome showing microcephaly, frontal

a,b: Patient A at 3 weeks; c,d: Patient B at 6 weeks, note the opening

MICROCEPHALY jo.pptx

Microcephaly - UF Health

Facial dysmorphism, skeletal anomalies, congenital glucoma, dysplastic nails: Mild Rubinstein-Taybi Syndrome - ScienceDirect

Congenital Malformations and Syndromes: Early Diagnosis and Prognosis in Neonatal Medicine