The Tatton-Brown-Rahman Syndrome: A clinical study of 55 individuals with de novo constitutive DNMT3A variants [version 1; referees: 3 approved]

  • Clinical Assessment of the Utility of Sequencing and Evaluation as a Service (CAUSES) Research Study
  • , Deciphering Developmental Disorders (DDD) Study
  • , Katrina Tatton-Brown (Lead / Corresponding author)
  • , Anna Zachariou
  • , Chey Loveday
  • , Anthony Renwick
  • , Shazia Mahamdallie
  • , Lise Aksglaede
  • , Diana Baralle
  • , Daniela Barge-Schaapveld
  • , Moira Blyth
  • , Mieke Bouma
  • , Jeroen Breckpot
  • , Beau Crabb
  • , Tabib Dabir
  • , Valerie Cormier-Daire
  • , Christine Fauth
  • , Richard Fisher
  • , Blanca Gener
  • , David Goudie
    • Tessa Homfray, Matthew Hunter, Agnete Jorgensen, Sarina G Kant, Cathy Kirally-Borri, David Koolen, Ajith Kumar, Anatalia Labilloy, Melissa Lees, Carlo Marcelis, Catherine Mercer, Cyril Mignot, Kathryn Miller, Katherine Neas, Ruth Newbury-Ecob, Daniela T Pilz, Renata Posmyk, Carlos Prada, Keri Ramsey, Linda M Randolph, Angelo Selicorni, Deborah Shears, Mohnish Suri, I. Karen Temple, Peter Turnpenny, Lionel Val Maldergem, Vinod Varghese, Hermine E Veenstra-Knol, Naomi Yachelevich, Laura Yates, Nazneen Rahman

Research output: Contribution to journal › Article › peer-review

86 Citations (Scopus)
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Medicine and Dentistry

Biochemistry, Genetics and Molecular Biology