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Rubinstein–Taybi syndrome: clinical and molecular overview | Expert Reviews  in Molecular Medicine | Cambridge Core
Rubinstein–Taybi syndrome: clinical and molecular overview | Expert Reviews in Molecular Medicine | Cambridge Core

Rubinstein-Taybi syndrome: MedlinePlus Genetics
Rubinstein-Taybi syndrome: MedlinePlus Genetics

Rubinstein-Taybi syndrome: MedlinePlus Genetics
Rubinstein-Taybi syndrome: MedlinePlus Genetics

Pitt–Hopkins syndrome - Wikiwand
Pitt–Hopkins syndrome - Wikiwand

Diagnostic analysis of the Rubinstein-Taybi syndrome: five cosmids should  be used for microdeletion detection and low number of protein truncating  mutations | Journal of Medical Genetics
Diagnostic analysis of the Rubinstein-Taybi syndrome: five cosmids should be used for microdeletion detection and low number of protein truncating mutations | Journal of Medical Genetics

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

List of skin conditions - Wikiwand
List of skin conditions - Wikiwand

Rubinstein-Taybi syndrome | pacs
Rubinstein-Taybi syndrome | pacs

Rubinstein-Taybi Syndrome: What therapies does Maria need?
Rubinstein-Taybi Syndrome: What therapies does Maria need?

First case report of inherited Rubinstein-Taybi syndrome associated with a  novel EP300 variant | BMC Medical Genetics | Full Text
First case report of inherited Rubinstein-Taybi syndrome associated with a novel EP300 variant | BMC Medical Genetics | Full Text

Diagnosis and management of Cornelia de Lange syndrome: first international  consensus statement. - Abstract - Europe PMC
Diagnosis and management of Cornelia de Lange syndrome: first international consensus statement. - Abstract - Europe PMC

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

Exon deletions of the EP300 and CREBBP genes in two children with Rubinstein –Taybi syndrome detected by aCGH | European Journal of Human Genetics
Exon deletions of the EP300 and CREBBP genes in two children with Rubinstein –Taybi syndrome detected by aCGH | European Journal of Human Genetics

Rubenstein-Taybi syndrome | Psychology Wiki | Fandom
Rubenstein-Taybi syndrome | Psychology Wiki | Fandom

Rubinstein-Taybi syndrome | pacs
Rubinstein-Taybi syndrome | pacs

Rubinstein-Taybi Syndrome: A Complete Overview — DermNet
Rubinstein-Taybi Syndrome: A Complete Overview — DermNet

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

Pediatric on Squares on X: "Rubinstein Taybi Syndrome #Pediatric #Genetics # syndrome https://t.co/OIJLNHKlSe" / X
Pediatric on Squares on X: "Rubinstein Taybi Syndrome #Pediatric #Genetics # syndrome https://t.co/OIJLNHKlSe" / X

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

22 Rubenstein-Taybi Syndrome ideas | syndrome, diagnosis, therapy
22 Rubenstein-Taybi Syndrome ideas | syndrome, diagnosis, therapy

Mosaic CREBBP mutation causes overlapping clinical features of Rubinstein– Taybi and Filippi syndromes | European Journal of Human Genetics
Mosaic CREBBP mutation causes overlapping clinical features of Rubinstein– Taybi and Filippi syndromes | European Journal of Human Genetics

Molecular studies in 10 cases of Rubinstein-Taybi syndrome, including a  mild variant showing a missense mutation in codon 1175 of CREBBP | Journal  of Medical Genetics
Molecular studies in 10 cases of Rubinstein-Taybi syndrome, including a mild variant showing a missense mutation in codon 1175 of CREBBP | Journal of Medical Genetics

Forgotten Diseases Research Foundation | Rubinstein-Taybi Syndrome (RTS)
Forgotten Diseases Research Foundation | Rubinstein-Taybi Syndrome (RTS)

Rubinstein-Taybi Syndrome: May 2013
Rubinstein-Taybi Syndrome: May 2013