Heterozygous rare variants in NR2F2 cause a recognizable multiple congenital anomaly syndrome with developmental delaysMythily Ganapathi, Elizabeth Bhoj, Leticia S. Matsuoka et al.|European Journal of Human Genetics|2023Cited by 25
Laboratory Predictors of Hemolytic Anemia in Patients With Systemic LoxoscelismJeremy W. Jacobs, Mary Ann Thompson, Lisa Bastarache|American Journal of Clinical Pathology|2021Cited by 12