Discovery of common Asian copy number variants using integrated high-resolution array CGH and massively parallel DNA sequencing
Hansoo Park(Brigham and Women's Hospital), Jong‐Il Kim(Seoul National University), Young Seok Ju(Seoul National University), Ömer Gökçümen(Brigham and Women's Hospital), Ryan E. Mills(Brigham and Women's Hospital), Sheehyun Kim(Seoul National University Hospital), Seungbok Lee(Seoul National University), Dongwhan Suh(Seoul National University), Dongwan Hong(Seoul National University Hospital), Hyunseok P. Kang(Seoul National University Hospital), Yun Joo Yoo(Seoul National University Hospital), Jong-Yeon Shin(Seoul National University Hospital), Hyun‐Jin Kim(Seoul National University), Maryam Yavartanoo(Seoul National University), Young Wha Chang(Seoul National University Hospital), Jung‐Sook Ha(Brigham and Women's Hospital), Wilson Chong(Brigham and Women's Hospital), Ga‐Ram Hwang(Brigham and Women's Hospital), Katayoon Darvishi(Brigham and Women's Hospital), Hye‐Ran Kim(Seoul National University), Song Ju Yang(Macrogen (South Korea)), Kap-Seok Yang(Macrogen (South Korea)), Hyungtae Kim(Seoul National University), Matthew E. Hurles(Wellcome Sanger Institute), Stephen W. Scherer(University of Toronto), Nigel P. Carter(Wellcome Sanger Institute), Chris Tyler‐Smith(Wellcome Sanger Institute), Charles Lee(Brigham and Women's Hospital), Jeong‐Sun Seo(Seoul National University)
Cited by 200Open Access