Genetic Heterogeneity in Rubinstein-Taybi Syndrome: Mutations in
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PDF] Genetic heterogeneity in Rubinstein-Taybi syndrome: mutations in both the CBP and EP300 genes cause disease.
Mosaic CREBBP mutation causes overlapping clinical features of Rubinstein–Taybi and Filippi syndromes
Rubinstein-Taybi Syndrome – New Indian Journal of Pediatrics
Microdeletions and mutations of CREBBP (CBP) gene can cause
Novel cAMP binding protein-BP (CREBBP) mutation in a girl with Rubinstein-Taybi syndrome, GH deficiency, Arnold Chiari malformation and pituitary hypoplasia – topic of research paper in Clinical medicine. Download scholarly article PDF
Rubinstein-Taybi Syndrome 1
Confirmation of EP300 gene mutations as a rare cause of Rubinstein–Taybi syndrome
Genes, Free Full-Text
Rubinstein-Taybi syndrome with scoliosis treated with single-stage posterior spinal fusion: illustrative case in: Journal of Neurosurgery: Case Lessons Volume 1 Issue 11 (2021) Journals
Localisation of nine CREBBP mutations (six of them of novel
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