Rubinstein–Taybi syndrome: clinical and molecular overview
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Deletion at chromosome 16p13.3 as a cause of Rubinstein-Taybi
Molecular studies in 10 cases of Rubinstein-Taybi syndrome
A case with Rubinstein-Taybi syndrome: A novel frameshift mutation
Rubinstein–Taybi syndrome in diverse populations - Tekendo
High frequency of copy number imbalances in Rubinstein–Taybi
First case report of inherited Rubinstein-Taybi syndrome
Rubinstein-Taybi Syndrome
Epigenetic mechanisms of Rubinstein-Taybi syndrome. - Abstract
PDF] Rubinstein-Taybi Syndrome in a 19-years old boy.
Molecular studies in 10 cases of Rubinstein-Taybi syndrome
Rubinstein-Taybi Syndrome: A Complete Overview — DermNet
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