Molecular studies in 10 cases of Rubinstein-Taybi syndrome, including a mild variant showing a missense mutation in codon 1175 of CREBBP

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Last updated 21 dezembro 2024
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
IJMS, Free Full-Text
Molecular studies in 10 cases of Rubinstein-Taybi syndrome, including a  mild variant showing a missense mutation in codon 1175 of CREBBP
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Molecular studies in 10 cases of Rubinstein-Taybi syndrome, including a  mild variant showing a missense mutation in codon 1175 of CREBBP
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Molecular studies in 10 cases of Rubinstein-Taybi syndrome, including a  mild variant showing a missense mutation in codon 1175 of CREBBP
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Molecular studies in 10 cases of Rubinstein-Taybi syndrome, including a  mild variant showing a missense mutation in codon 1175 of CREBBP
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Molecular studies in 10 cases of Rubinstein-Taybi syndrome, including a  mild variant showing a missense mutation in codon 1175 of CREBBP
IJMS, Free Full-Text
Molecular studies in 10 cases of Rubinstein-Taybi syndrome, including a  mild variant showing a missense mutation in codon 1175 of CREBBP
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Molecular studies in 10 cases of Rubinstein-Taybi syndrome, including a  mild variant showing a missense mutation in codon 1175 of CREBBP
PDF) Clinical exome sequencing identifies novel CREBBP variants in
Molecular studies in 10 cases of Rubinstein-Taybi syndrome, including a  mild variant showing a missense mutation in codon 1175 of CREBBP
PDF) Molecular studies in 10 cases of 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
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Molecular studies in 10 cases of Rubinstein-Taybi syndrome, including a  mild variant showing a missense mutation in codon 1175 of CREBBP
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Molecular studies in 10 cases of Rubinstein-Taybi syndrome, including a  mild variant showing a missense mutation in codon 1175 of CREBBP
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