4 Newborn with Rubinstein-Taybi syndrome showing microcephaly
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High frequency of copy number imbalances in Rubinstein–Taybi patients negative to CREBBP mutational analysis
Facial dysmorphism, skeletal anomalies, congenital glucoma, dysplastic nails: Mild Rubinstein-Taybi Syndrome - ScienceDirect
Microcephaly: Causes, Complications, and Diagnosis
Rubinstein-Taybi Syndrome 1
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
Facial dysmorphism, skeletal anomalies, congenital glucoma, dysplastic nails: Mild Rubinstein-Taybi Syndrome - ScienceDirect
An approach to a chil with microcephaly
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
Fetal phenotype of Rubinstein‐Taybi syndrome caused by CREBBP mutations - Van‐Gils - 2019 - Clinical Genetics - Wiley Online Library
Rubinstein–Taybi Syndrome in a Filipino Infant with a Novel CREBBP Gene Pathogenic Variant
CREBBP mutations in individuals without Rubinstein–Taybi syndrome phenotype - Menke - 2016 - American Journal of Medical Genetics Part A - Wiley Online Library
Hands and feet in RTS. Broad thumbs, broad terminal phalanges were seen.
4 Newborn with Rubinstein-Taybi syndrome showing microcephaly, frontal
MICROCEPHALY jo.pptx
Microcephaly MedLink Neurology
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