Somatic mutations and progressive monosomy modify SAMD9-related phenotypes in humans
Federica Buonocore(Institute of Child Health), John C. Achermann(Institute of Child Health), Miriam Erlacher(University Medical Center Freiburg), Paolo Ghirri(University of Pisa), Marcin W. Włodarski(St. Jude Children's Research Hospital), Peter Kühnen(Humboldt-Universität zu Berlin), Annie Procter(University Hospital of Wales), Jenifer P. Suntharalingham(University College London), Brigitte Strahm(University Medical Center Freiburg), J K Wales(Royal Hallamshire Hospital), Annette Grüters(Unknown), Dieter Knöbl(Karlsruhe University of Education), Deborah Morrogh(Great Ormond Street Hospital for Children NHS Foundation Trust), Glenn Anderson(Great Ormond Street Hospital), Shane McKee(Belfast City Hospital), Oliver Blankenstein(Inserm), Martin Digweed(Charité - Universitätsmedizin Berlin), Mohammed Didi(Alder Hey Children's NHS Foundation Trust), Dale Moulding(Great Ormond Street Hospital), Wei Chen(Max Delbrück Center), Charlotte M. Niemeyer(University of Freiburg), George Kokai(Alder Hey Children's NHS Foundation Trust), Noushafarin Khajavi(Institute of Experimental Endocrinology of the Slovak Academy of Sciences), Paul Dimitri(University of Sheffield), Angela F. Brady(Northwick Park Hospital), Harald Stachelscheid(Berlin Institute of Health at Charité - Universitätsmedizin Berlin)
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