Back to matchesWe found a matchYour institution may have access to this item. Find your institution then sign in to continue.TitleSyndromic inherited poikiloderma due to a de novo mutation in FAM111B.AuthorsTakeichi, T.; Nanda, A.; Yang, H. ‐ S.; Hsu, C. ‐ K.; Lee, J.Y. ‐ Y.; Al ‐ Ajmi, H.; Akiyama, M.; Simpson, M.A.; McGrath, J.A.AbstractThe article discusses a case of syndromic inherited poikiloderma due to a de novo mutation in FAM111B gene.SubjectsROTHMUND-Thomson syndrome; GENESPublicationBritish Journal of Dermatology, 2017, Vol 176, Issue 2, p534ISSN0007-0963Publication typeArticleDOI10.1111/bjd.14845