CREBBP and EP300 mutational spectrum and clinical presentations in a cohort of Swedish patients with Rubinstein–Taybi syndrome - Wincent - 2016 - Molecular Genetics & Genomic Medicine - Wiley Online Library
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Rubinstein-Taybi Syndrome and Epigenetic Alterations. - Abstract - Europe PMC
New insights into genetic variant spectrum and genotype–phenotype correlations of Rubinstein‐Taybi syndrome in 39 CREBBP‐positive patients - Pérez‐Grijalba - 2019 - Molecular Genetics & Genomic Medicine - Wiley Online Library
Epigenetic mechanisms of Rubinstein-Taybi syndrome. - Abstract - Europe PMC
Exon deletions of the EP300 and CREBBP genes in two children with Rubinstein –Taybi syndrome detected by aCGH
Rubinstein-Taybi Syndrome and Epigenetic Alterations
Analysis of mutations within the intron20 splice donor site of CREBBP in patients with and without classical RSTS
Further delineation of an entity caused by CREBBP and EP300 mutations but not resembling Rubinstein–Taybi syndrome - Menke - 2018 - American Journal of Medical Genetics Part A - Wiley Online Library
PDF) Missense Variants in the Histone Acetyltransferase Complex Component Gene TRRAP Cause Autism and Syndromic Intellectual Disability
SIOP 2016 Scientific Programme+Index - 2016 - Pediatric Blood & Cancer - Wiley Online Library
Textbook On Scar Management-Téot-2021, PDF, Small Interfering Rna
Rubinstein-Taybi Syndrome and Epigenetic Alterations
Chapters Archive - Page 38 of 44 - Endotext
PDF) Utilization of Whole Exome Sequencing to Identify Causative Mutations in Familial Congenital Heart Disease
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