A de novo SATB2 mutation in monozygotic twins with cleft palate, dental anomalies, and developmental delay.
Schwartz, E; Wilkens, A; Noon, SE; Krantz, ID; Wu, Y.
American Journal of Medical Genetics, Part A.
2017;
173:809-812.
Hearing loss, coloboma and left ventricular enlargement in a boy with an interstitial 10q26 deletion.
Ramos, M; Wilkens, A; Krantz, ID; Wu, Y.
American Journal of Medical Genetics, Part C: Seminars in Medical Genetics.
2016;
172:109-116.
A de novo interstitial deletion of 7q31.2q31.31 identified in a girl with developmental delay and hearing loss.
Zhao, J; Noon, SE; Krantz, ID; Wu, Y.
American Journal of Medical Genetics, Part C: Seminars in Medical Genetics.
2016;
172:102-108.