Rubinstein–Taybi syndrome in diverse populations - Tekendo
Por um escritor misterioso
Last updated 24 setembro 2024
Identification of 22q11.2 deletion in a patient with schizophrenia and clinically diagnosed Rubinstein–Taybi syndrome - Nagai - 2022 - Psychiatry and Clinical Neurosciences Reports - Wiley Online Library
PDF) Rubinstein-Taybi Syndrome: A Case Report
Identification of 22q11.2 deletion in a patient with schizophrenia and clinically diagnosed Rubinstein–Taybi syndrome - Nagai - 2022 - Psychiatry and Clinical Neurosciences Reports - Wiley Online Library
A novel CREBBP mutation and its phenotype in a case of Rubinstein–Taybi syndrome, BMC Medical Genomics
Rubinstein–Taybi syndrome in diverse populations - Tekendo‐Ngongang - 2020 - American Journal of Medical Genetics Part A - Wiley Online Library
PDF) Rubinstein-Taybi syndrome with normal FISH result and CREBBP gene analysis: A case report
PDF) Exon deletions of the EP300 and CREBBP genes in two children with Rubinstein-Taybi syndrome detected by aCGH
PDF) Genetic and clinical heterogeneity in Korean patients with Rubinstein–Taybi syndrome
Genes, Free Full-Text
Facial features and limb anomalies of all the patients: a Facial
Wiley Special Collection on African Genomics: American Journal of Medical Genetics Part A
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