Molecular studies in 10 cases of Rubinstein-Taybi syndrome

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Molecular studies in 10 cases of Rubinstein-Taybi syndrome
A case of bilateral elbow dislocation in a patient with Rubinstein-Taybi syndrome - JSES International
Molecular studies in 10 cases of Rubinstein-Taybi syndrome
Multiple pilomatricomas in twins with Rubinstein-Taybi syndrome
Molecular studies in 10 cases of Rubinstein-Taybi syndrome
PDF) Rubinstein-Taybi syndrome with normal FISH result and CREBBP gene analysis: A case report
Molecular studies in 10 cases of Rubinstein-Taybi syndrome
Rubinstein-Taybi syndrome with scoliosis – topic of research paper in Clinical medicine. Download scholarly article PDF and read for free on CyberLeninka open science hub.
Molecular studies in 10 cases of Rubinstein-Taybi syndrome
Genetic heterogeneity in Rubinstein–Taybi syndrome: delineation of the phenotype of the first patients carrying mutations in EP300
Molecular studies in 10 cases of Rubinstein-Taybi syndrome
Diagnostic analysis of the Rubinstein-Taybi syndrome: five cosmids should be used for microdeletion detection and low number of protein truncating mutations
Molecular studies in 10 cases of Rubinstein-Taybi syndrome
Rubinstein-Taybi Syndrome
Molecular studies in 10 cases of Rubinstein-Taybi syndrome
Frontiers Case report: A preterm infant with rubinstein-taybi syndrome and Marmorata telangiectatica harboring a frameshift mutation in the CREBBP gene
Molecular studies in 10 cases of Rubinstein-Taybi syndrome
Rubinstein-Taybi Syndrome
Molecular studies in 10 cases of Rubinstein-Taybi syndrome
Adults with Rubinstein–Taybi syndrome - Stevens - 2011 - American Journal of Medical Genetics Part A - Wiley Online Library
Molecular studies in 10 cases of Rubinstein-Taybi syndrome
Prediction of an RTI deletion using selected Rubinstein-Taybi syndrome
Molecular studies in 10 cases of Rubinstein-Taybi syndrome
Clinical and molecular findings of the six patients with Rubinstein
Molecular studies in 10 cases of Rubinstein-Taybi syndrome
Mosaic CREBBP mutation causes overlapping clinical features of Rubinstein– Taybi and Filippi syndromes
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