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

PDF) Molecular studies in 10 cases of Rubinstein-Taybi syndrome

CREBBP mutations in individuals without Rubinstein–Taybi syndrome

Characterization of 14 novel deletions underlying Rubinstein–Taybi

Rubinstein-Taybi Syndrome: spectrum of CREBBP mutations in Italian

Insights into genotype–phenotype correlations from CREBBP point

PDF) FISH studies in 45 patients with Rubinstein-Taybi syndrome

Frontiers Case Report: Low-Level Maternal Mosaicism of a Novel

Molecular studies in 10 cases of Rubinstein-Taybi syndrome

PDF) Lacrimal drainage anomalies in Rubinstein-Taybi syndrome

Two adults with Rubinstein–Taybi syndrome with mild mental
Chromosome 16p13.3 Contiguous Gene Deletion Syndrome including the

PDF) Spectrum of CREBBP mutations in Indian patients with

Diagnostic analysis of the Rubinstein-Taybi syndrome: five cosmids

Rubinstein-Taybi Syndrome

Rubinstein–Taybi syndrome: clinical and molecular overview
de
por adulto (o preço varia de acordo com o tamanho do grupo)