Evaluating whole genome sequencing for rare diseases in newborn screening: evidence synthesis from a series of systematic reviews
评估新生儿筛查中罕见病的全基因组测序:一系列系统评价的证据综合
期刊:Health Technology Assessment
影响因子:4
doi:10.3310/DJRF1124
Freeman, Karoline; Dinnes, Jacqueline; Shinkins, Bethany; Clark, Corinna; Kander, Inès; Scandrett, Katie; Chockalingam, Shivashri; Osman, Aziza; Dracup, Naila; Court, Rachel; Butt, Furqan; Visintin, Cristina; Bonham, James R; Elliman, David; Shortland, Graham; Mackie, Anne; Miedzybrodzka, Zosia; Morgan, Sian M; Boardman, Felicity; Takwoingi, Yemisi; Taylor-Phillips, Sian