Alexandra Falsey

Discordant clinical phenotype in monozygotic twins with Alagille syndrome: Possible influence of non‐genetic factors

N. Spinner, Tomohiko Nakamura, Y. Ogiso, 2016, American journal of medical genetics. Part A.

Heterozygous Deletion of FOXA2 Segregates with Disease in a Family with Heterotaxy, Panhypopituitarism, and Biliary Atresia

I. Krantz, N. Spinner, M. Devoto, 2015, Human mutation.

Exome sequencing reveals compound heterozygous mutations in ATP8B1 in a JAG1/NOTCH2 mutation‐negative patient with clinically diagnosed Alagille syndrome

I. Krantz, N. Spinner, M. Devoto, 2015, American journal of medical genetics. Part A.

Compound heterozygous mutations in NEK8 in siblings with end‐stage renal disease with hepatic and cardiac anomalies

N. Spinner, K. Coleman, M. Devoto, 2016, American journal of medical genetics. Part A.