Rubinstein–Taybi syndrome: clinical and molecular overview
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PDF] Rubinstein-Taybi Syndrome Associated with Pituitary

Analysis of mutations within the intron20 splice donor site of

Frontiers Genetic Diagnosis of Rubinstein–Taybi Syndrome With

CREBBP and EP300 mutational spectrum and clinical presentations in

Rubinstein–Taybi syndrome in diverse populations - Tekendo

PDF) HEPATOBLASTOMA WITH RUBINSTEIN-TAYBI SYNDROME: A RARE ASSOCIATION

Rubinstein-Taybi Syndrome

Rubinstein–Taybi syndrome: clinical and molecular overview

EP300‐related Rubinstein–Taybi syndrome: Highlighted rare

Characterization of 14 novel deletions underlying Rubinstein–Taybi

High frequency of copy number imbalances in Rubinstein–Taybi

Novel cAMP binding protein-BP (CREBBP) mutation in a girl with

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Deletion at chromosome 16p13.3 as a cause of Rubinstein-Taybi

Molecular studies in 10 cases of Rubinstein-Taybi syndrome
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