Casarubinstein síndrome

Molecular studies in 10 cases of Rubinstein-Taybi syndrome

Por um escritor misterioso
Last updated 20 março 2025
Molecular studies in 10 cases of Rubinstein-Taybi syndrome
Molecular studies in 10 cases of Rubinstein-Taybi syndrome
Prediction of an RTI deletion using selected Rubinstein-Taybi syndrome
Molecular studies in 10 cases of Rubinstein-Taybi syndrome
Psychiatric Profile in Rubinstein-Taybi Syndrome
Molecular studies in 10 cases of Rubinstein-Taybi syndrome
Rubinstein-Taybi syndrome: MedlinePlus Genetics
Molecular studies in 10 cases of Rubinstein-Taybi syndrome
Rubinstein-Taybi syndrome: clinical features, genetic basis, diagnosis, and management, Italian Journal of Pediatrics
Molecular studies in 10 cases of Rubinstein-Taybi syndrome
Rubinstein-Taybi syndrome in a Saudi boy with distinct features and variants in both the CREBBP and EP300 genes: a case report, BMC Medical Genetics
Molecular studies in 10 cases of Rubinstein-Taybi syndrome
Rubinstein-Taybi syndrome in a Saudi boy with distinct features and variants in both the CREBBP and EP300 genes: a case report, BMC Medical Genetics
Molecular studies in 10 cases of Rubinstein-Taybi syndrome
Genes, Free Full-Text
Molecular studies in 10 cases of Rubinstein-Taybi syndrome
Characterization of 14 novel deletions underlying Rubinstein–Taybi syndrome: an update of the CREBBP deletion repertoire
Molecular studies in 10 cases of Rubinstein-Taybi syndrome
Diagnostic analysis of the Rubinstein-Taybi syndrome: five cosmids should be used for microdeletion detection and low number of protein truncating mutations
Molecular studies in 10 cases of Rubinstein-Taybi syndrome
Dysmorphic and skeletal features of Rubinstein‐Taybi syndrome patients.
Molecular studies in 10 cases of Rubinstein-Taybi syndrome
Psychiatric Profile in Rubinstein-Taybi Syndrome
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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