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
Last updated 04 janeiro 2025
Molecular studies in 10 cases of Rubinstein-Taybi syndrome, including a  mild variant showing a missense mutation in codon 1175 of CREBBP
Molecular studies in 10 cases of Rubinstein-Taybi syndrome, including a  mild variant showing a missense mutation in codon 1175 of CREBBP
Rubinstein-Taybi syndrome in a Saudi boy with distinct features
Molecular studies in 10 cases of Rubinstein-Taybi syndrome, including a  mild variant showing a missense mutation in codon 1175 of CREBBP
Genetic Heterogeneity in Rubinstein-Taybi Syndrome: Mutations in
Molecular studies in 10 cases of Rubinstein-Taybi syndrome, including a  mild variant showing a missense mutation in codon 1175 of CREBBP
PDF) FISH studies in 45 patients with Rubinstein-Taybi syndrome
Molecular studies in 10 cases of Rubinstein-Taybi syndrome, including a  mild variant showing a missense mutation in codon 1175 of CREBBP
Rubinstein-Taybi Syndrome
Molecular studies in 10 cases of Rubinstein-Taybi syndrome, including a  mild variant showing a missense mutation in codon 1175 of CREBBP
Rubinstein-Taybi Syndrome
Molecular studies in 10 cases of Rubinstein-Taybi syndrome, including a  mild variant showing a missense mutation in codon 1175 of CREBBP
PDF] Chromosome 16p13.3 Contiguous Gene Deletion Syndrome
Molecular studies in 10 cases of Rubinstein-Taybi syndrome, including a  mild variant showing a missense mutation in codon 1175 of CREBBP
Rubinstein–Taybi syndrome: clinical and molecular overview
Molecular studies in 10 cases of Rubinstein-Taybi syndrome, including a  mild variant showing a missense mutation in codon 1175 of CREBBP
Rubinstein-Taybi syndrome in a Saudi boy with distinct features
Molecular studies in 10 cases of Rubinstein-Taybi syndrome, including a  mild variant showing a missense mutation in codon 1175 of CREBBP
CREBBP mutations in individuals without Rubinstein–Taybi syndrome
Molecular studies in 10 cases of Rubinstein-Taybi syndrome, including a  mild variant showing a missense mutation in codon 1175 of CREBBP
CREBBP mutations in individuals without Rubinstein–Taybi syndrome

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