Xq22 deletions and correlation with distinct neurological disease traits in females: Further evidence for a contiguous gene syndrome
Hadia Hijazi(Baylor College of Medicine), James R. Lupski(Baylor College of Medicine), Andrea Poretti(Johns Hopkins University), Angelique Davis‐Williams(Alfred I. duPont Hospital for Children), Davut Pehli̇van(Baylor College of Medicine), Laura Bernardini(Casa Sollievo della Sofferenza), P.A.L. Wight(University of Arkansas for Medical Sciences), Michael J. Friez(Greenwood Genetic Center), Julie R. Jones(Greenwood Genetic Center), Jennifer R. Taube(Alfred I. duPont Hospital for Children), Pankaj Patyal(Institute on Aging), Sau Wai Cheung(Chinese University of Hong Kong), Carly Jornlin(Alfred I. duPont Hospital for Children), Soe Mar(St. Louis Children's Hospital), Bárbara Torres(Johannes Gutenberg University Mainz), Claudia Gonzaga‐Jauregui(Case Western Reserve University), Ken Inoue(University of California San Diego), Claudia M.B. Carvalho(Pacific Northwest Diabetes Research Institute), Grace M. Hobson(DuPont (United States)), Feng Zhang(Affiliated Hospital of North Sichuan Medical College), Jennifer A. Lee(Greenwood Genetic Center), Ping Fang(Beijing Institute of Technology), Andrea Hanson‐Kahn(Stanford Health Care), Xiaofei Song(Jiangsu University), SakkuBai Naidu(Kennedy Krieger Institute), Thomas Alberico(Alfred I. duPont Hospital for Children), Melanie A. Manning(Stanford University), Fernanda S. Coelho(Fundação Oswaldo Cruz), Siddharth Srivastava(Boston Children's Hospital)
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