학술논문
Heterozygous rare variants in NR2F2 cause a recognizable multiple congenital anomaly syndrome with developmental delays
Document Type
Article
Author
Ganapathi, M.; Thomas-Wilson, A.; Matsuoka, L.S.; March, M.; Li, D.; Zackai, E.; Bhoj, E.; Brokamp, E.; Benito-Sanz, S.; White, S.M.; Lachlan, K.; Ahimaz, P.; Sewda, A.; Schacht, J.P.; Iglesias, A.D.; Chung, W.K.; Bastarache, L.; Stoler, J.M.; Lucia, S.; Bramswig, N.C.; Schmetz, A.; Baptista, J.; Stals, K.; Demurger, F.; Cogne, B.; Isidor, B.; Bedeschi, M.F.; Peron, A.; Amiel, J.; Gordon, C.T.; Morton, J.; Seidel, V.; Baskin, S.M.; Thiffault, I.; Cogan, J.D.; Bowdin, S.; Cogan, J.D.
Source
In: European Journal of Human Genetics . (European Journal of Human Genetics, October 2023, 31(10):1117-1124)
Subject
Language
English
ISSN
14765438
10184813
10184813