학술논문
Exome-wide assessment of isolated biliary atresia: A report from the National Birth Defects Prevention Study using child–parent trios and a case–control design to identify novel rare variants
Document Type
Article
Author
Sok, P.; Brown, A.L.; Schraw, J.M.; Harpavat, S.; Lupo, P.J.; Sabo, A.; Dugan-Perez, S.; Gibbs, R.A.; Meng, Q.; Muzny, D.; Almli, L.M.; Jenkins, M.M.; Moore, C.A.; Reefhuis, J.; Nembhard, W.N.; Agopian, A.J.; Bamshad, M.J.; Chong, J.X.; Blue, E.E.; Brody, L.C.; Mullikin, J.C.; Pangilinan, F.; Browne, M.L.; Canfield, M.A.; Carmichael, S.L.; Shaw, G.M.; Feldkamp, M.L.; Finnell, R.H.; Lei, Y.; Kay, D.M.; Olshan, A.F.; Romitti, P.A.; Werler, M.M.
Source
In: American Journal of Medical Genetics, Part A . (American Journal of Medical Genetics, Part A, June 2023, 191(6):1546-1556)
Subject
Language
English
ISSN
15524833
15524825
15524825