论文信息 - Copy number variant and runs of homozygosity detection by microarrays enabled more precise molecular diagnoses in 11,020 clinical exome cases - 字舞流文

Copy number variant and runs of homozygosity detection by microarrays enabled more precise molecular diagnoses in 11,020 clinical exome cases

P. Stankiewicz | A. Breman | Ankita Patel | C. Shaw | J. Lupski | S. Cheung | R. Gibbs | A. Beaudet | D. Muzny | S. Lalani | Yaping Yang | P. Ward | F. Xia | J. Scull | C. Eng | R. Ghosh | J. Posey | P. Liu | W. Bi | C. Bacino | T. Chiang | Avinash V. Dharmadhikari | Francesco Vetrini | Bo Yuan | Linyan Meng | Weimin He | Shen Gu | Rui Xiao | Amy M. Breman | Janice L. Smith | Xia Wang | Hongzheng Dai | Pengfei Liu | Chunjing Qu | Alicia A. Braxton | Sami Al Masri | Allen H. Jiang