Rubinstein–Taybi syndrome in diverse populations - Tekendo
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Descrição
Rubinstein-Taybi syndrome due to CREBBP mutations (Concept Id: C4551859)
Nuclear Localization signals (NLSs) predicted by PSORTII [21] analysis.
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
Rubinstein-Taybi syndrome: principal oral and dental disorders and literature update
RT-PCR and bioinformatic analysis of the splice site mutation
Characteristic facial appearance with downward slant of palpebral
Psychiatric Profile in Rubinstein-Taybi Syndrome
Otopalatodigital Syndrome, Type Ii disease: Malacards - Research Articles, Drugs, Genes, Clinical Trials
PDF) Rubinstein–Taybi syndrome 2 with cerebellar abnormality and neural tube defect
Summary of deletion results. (a) Large deletions. A schematic
Genes, Free Full-Text
Genes, Free Full-Text
Rubinstein–Taybi syndrome in diverse populations - Tekendo‐Ngongang - 2020 - American Journal of Medical Genetics Part A - Wiley Online Library
PDF) Second report of slipped capital femoral epiphysis in Rubinstein-Taybi syndrome
Characterization of CREBBP gene dosage anomalies by QMF-PCR
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