Tatton-Brown–Rahman syndrome (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Tatton-Brown–Rahman syndrome" in English language version.

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pubmed.ncbi.nlm.nih.gov

  • Ostrowski PJ, Tatton-Brown K (2022-06-30). Adam MP, Feldman J, Mirzaa GM, et al. (eds.). "Tatton-Brown-Rahman Syndrome". GeneReviews. University of Washington, Seattle. PMID 35771960. Retrieved 2024-01-09.
  • Tatton-Brown K, Seal S, Ruark E, Harmer J, Ramsay E, et al. (2014). "Mutations in the DNA methyltransferase gene DNMT3A cause an overgrowth syndrome with intellectual disability". Nat Genet. 46 (4): 385–8. doi:10.1038/ng.2917. PMC 3981653. PMID 24614070.
  • Tatton-Brown K, Zachariou A, Loveday C, Renwick A, Mahamdallie S, et al. (2018). "The Tatton-Brown-Rahman Syndrome: A clinical study of 55 individuals with de novo constitutive DNMT3A variants". Wellcome Open Research. 3: 46. doi:10.12688/wellcomeopenres.14430.1. PMC 5964628. PMID 29900417.
  • Jiménez de la Peña M, Rincón-Pérez I, López-Martín S, Albert J, Martín Fernández-Mayoralas D, Fernández-Perrone AL, et al. (2023). "Tatton-Brown-Rahman syndrome: Novel pathogenic variants and new neuroimaging findings". Am J Med Genet A. 194 (2): 211–217. doi:10.1002/ajmg.a.63434. PMID 37795572.
  • Hamagami N, Wu DY, Clemens AW, Nettles SA, Li A, Gabel HW (2023). "NSD1 deposits histone H3 lysine 36 dimethylation to pattern non-CG DNA methylation in neurons". Mol Cell. 83 (9): 1412–1428.e7. doi:10.1016/j.molcel.2023.04.001. PMC 10230755. PMID 37098340.

ncbi.nlm.nih.gov

  • Ostrowski PJ, Tatton-Brown K (2022-06-30). Adam MP, Feldman J, Mirzaa GM, et al. (eds.). "Tatton-Brown-Rahman Syndrome". GeneReviews. University of Washington, Seattle. PMID 35771960. Retrieved 2024-01-09.
  • Tatton-Brown K, Seal S, Ruark E, Harmer J, Ramsay E, et al. (2014). "Mutations in the DNA methyltransferase gene DNMT3A cause an overgrowth syndrome with intellectual disability". Nat Genet. 46 (4): 385–8. doi:10.1038/ng.2917. PMC 3981653. PMID 24614070.
  • Tatton-Brown K, Zachariou A, Loveday C, Renwick A, Mahamdallie S, et al. (2018). "The Tatton-Brown-Rahman Syndrome: A clinical study of 55 individuals with de novo constitutive DNMT3A variants". Wellcome Open Research. 3: 46. doi:10.12688/wellcomeopenres.14430.1. PMC 5964628. PMID 29900417.
  • Hamagami N, Wu DY, Clemens AW, Nettles SA, Li A, Gabel HW (2023). "NSD1 deposits histone H3 lysine 36 dimethylation to pattern non-CG DNA methylation in neurons". Mol Cell. 83 (9): 1412–1428.e7. doi:10.1016/j.molcel.2023.04.001. PMC 10230755. PMID 37098340.