The Tatton-Brown-Rahman Syndrome: A clinical study of 55 individuals with de novo constitutive DNMT3A variants
塔顿-布朗-拉赫曼综合征:一项针对55名携带新生DNMT3A基因突变个体的临床研究
期刊:Wellcome Open Research
影响因子:
doi:10.12688/wellcomeopenres.14430.1
Tatton-Brown, Katrina; Zachariou, Anna; Loveday, Chey; Renwick, Anthony; Mahamdallie, Shazia; Aksglaede, Lise; Baralle, Diana; Barge-Schaapveld, Daniela; Blyth, Moira; Bouma, Mieke; Breckpot, Jeroen; Crabb, Beau; Dabir, Tabib; Cormier-Daire, Valerie; Fauth, Christine; Fisher, Richard; Gener, Blanca; Goudie, David; Homfray, Tessa; Hunter, Matthew; Jorgensen, Agnete; Kant, Sarina G; Kirally-Borri, Cathy; Koolen, David; Kumar, Ajith; Labilloy, Anatalia; Lees, Melissa; Marcelis, Carlo; Mercer, Catherine; Mignot, Cyril; Miller, Kathryn; Neas, Katherine; Newbury-Ecob, Ruth; Pilz, Daniela T; Posmyk, Renata; Prada, Carlos; Ramsey, Keri; Randolph, Linda M; Selicorni, Angelo; Shears, Deborah; Suri, Mohnish; Temple, I Karen; Turnpenny, Peter; Val Maldergem, Lionel; Varghese, Vinod; Veenstra-Knol, Hermine E; Yachelevich, Naomi; Yates, Laura; Rahman, Nazneen