Rubinstein–Taybi syndrome: clinical and molecular overview
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Rubinstein–Taybi syndrome: clinical and molecular overview
Congenital glaucoma as a presenting feature of Rubinstein-Taybi
CBP-HSF2 structural and functional interplay in Rubinstein-Taybi
Genetic heterogeneity in Rubinstein–Taybi syndrome: delineation of
Case report: a Chinese girl like atypical Rubinstein–Taybi
Rubinstein-Taybi Syndrome
Analysis of mutations within the intron20 splice donor site of
Deletion at chromosome 16p13.3 as a cause of Rubinstein-Taybi
Frontiers Genetic Diagnosis of Rubinstein–Taybi Syndrome With
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