Rubinstein-Taybi Syndrome
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The Ridenour Family - RareKC
Rubinstein-Taybi Syndrome: A Complete Overview — DermNet
Congenital glaucoma as a presenting feature of Rubinstein-Taybi syndrome in an infant with a novel pathogenic variant in the CREBBP gene
Rubinstein-Taybi Syndrome
Molecular studies in 10 cases of Rubinstein-Taybi syndrome, including a mild variant showing a missense mutation in codon 1175 of CREBBP
A Case of Rubinstein-Taybi Syndrome with Tetralogy of Fallot
Learning to Speak at Age 18 with a Sister Who Never Quits (Rubinstein-Taybi Syndrome)
Rubinstein-Taybi syndrome in a Saudi boy with distinct features and variants in both the CREBBP and EP300 genes: a case report, BMC Medical Genetics
Rubinstein-Taybi Syndrome
Rubinstein-Taybi Syndrome: A case report
Rubinstein–Taybi syndrome - Wikipedia