Molecular studies in 10 cases of Rubinstein-Taybi syndrome, including a mild variant showing a missense mutation in codon 1175 of CREBBP
Por um escritor misterioso
Descrição
Diagnostic analysis of the Rubinstein-Taybi syndrome: five cosmids
High frequency of copy number imbalances in Rubinstein–Taybi
Opposing Effects of CREBBP Mutations Govern the Phenotype of
Rubinstein-Taybi Syndrome
Structure of CBP and p300. The CBP protein is composed of 2442
PDF) Rubinstein-Taybi syndrome medical guidelines
Rubinstein-Taybi Syndrome
Rubinstein-Taybi Syndrome: spectrum of CREBBP mutations in Italian
PDF) Spectrum of CREBBP mutations in Indian patients with
A novel CREBBP mutation and its phenotype in a case of Rubinstein
Genes, Free Full-Text
PDF) Molecular studies in 10 cases of Rubinstein-Taybi syndrome
de
por adulto (o preço varia de acordo com o tamanho do grupo)