RUBINSTEIN TAYBI SYNDROME An autosomal dominant disease associated
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Molecular studies in 10 cases of Rubinstein-Taybi syndrome, including a mild variant showing a missense mutation in codon 1175 of CREBBP
Genetic Heterogeneity in Rubinstein-Taybi Syndrome: Mutations in Both the CBP and EP300 Genes Cause Disease - ScienceDirect
Multiple pilomatricomas in twins with Rubinstein-Taybi syndrome
Rubinstein–Taybi syndrome - Wikipedia
Figure 1 from Rubinstein-Taybi Syndrome in a 19-years old boy.
Frontiers Case report: A preterm infant with rubinstein-taybi syndrome and Marmorata telangiectatica harboring a frameshift mutation in the CREBBP gene
Rubinstein-Taybi Syndrome Awareness
Rubinstein–Taybi syndrome: clinical and molecular overview, Expert Reviews in Molecular Medicine
Rubinstein-Taybi Syndrome: A Complete Overview — DermNet
IJMS, Free Full-Text
Rubinstein-Taybi Syndrome: Symptoms, Causes, Treatment
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