Rubinstein–Taybi syndrome in diverse populations - Tekendo
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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
Wiley Special Collection on African Genomics: American Journal of Medical Genetics Part A
A novel CREBBP mutation and its phenotype in a case of Rubinstein–Taybi syndrome, BMC Medical Genomics
PDF) Exon deletions of the EP300 and CREBBP genes in two children with Rubinstein-Taybi syndrome detected by aCGH
Genes, Free Full-Text
Expanding the genotypic and phenotypic spectrum in a diverse cohort of 104 individuals with Wiedemann‐Steiner syndrome - Sheppard - 2021 - American Journal of Medical Genetics Part A - Wiley Online Library
PDF) Rubinstein-Taybi syndrome: principal oral and dental disorders and literature update
PDF) Rubinstein-Taybi Syndrome: A Model of Epigenetic Disorder
cDNA probes used to study the CBP gene in RTS patients
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