Martin, Carol-AnneSarlós, KataLogan, Clare VThakur, Roshan SinghParry, David ABizard, Anna HLeitch, AndreaCleal, LouiseAli, Nadia ShaukatAl-Owain, Mohammed AAllen, WilliamAltmüller, JanineAza-Carmona, MiriamBarakat, Bushra AYBarraza-García, JimenaBegtrup, AmberBogliolo, MassimoCho, Megan TCruz-Rojo, JaimeDhahrabi, Hassan Ali MundiElcioglu, Nursel HGOSgeneGorman, Gráinne SJobling, RebekahKesterton, IanKishita, YoshihitoKohda, MasakazuLe Quesne Stabej, PolonaMalallah, Asam JassimNürnberg, PeterOhtake, AkiraOkazaki, YasushiPujol, RoserRamirez, Maria JoséRevah-Politi, AnyaShimura, MasaruStevens, PaulTaylor, Robert WTurner, LesleyWilliams, HywelWilson, CarolynYigit, GökhanZahavich, LauraAlkuraya, Fowzan SSurralles, JordiIglesias, AlejandroMurayama, KeiWollnik, BerndDattani, MehulHeath, Karen EHickson, Ian DJackson, Andrew P2020-07-102018-09American journal of human genetics 103(3):456 Sep 20180002-9297https://hdl.handle.net/2292/52397PrintItems in ResearchSpace are protected by copyright, with all rights reserved, unless otherwise indicated. Previously published items are made available in accordance with the copyright policy of the publisher.https://researchspace.auckland.ac.nz/docs/uoa-docs/rights.htmhttps://creativecommons.org/licenses/by-nc-nd/4.0/GOSgeneMutations in TOP3A Cause a Bloom Syndrome-like Disorder.Journal Article10.1016/j.ajhg.2018.08.012Copyright: The authorshttp://purl.org/eprint/accessRights/OpenAccess1537-6605