Whole-exome sequencing for diagnosis of Peters-plus syndrome after prenatal diagnosis of recurrent low PAPP-A and multiple fetal anomalies in two consecutive pregnancies.

Authors

P Kamalapathy
Jill S. Fonda Allen, George Washington University
Charles J. Macri, George Washington University
Anne K. Lawrence, George Washington University
Debra S. Regier, George Washington University
Eva Rubio, George Washington University

Document Type

Journal Article

Publication Date

5-7-2019

Journal

Journal of Neonatal Perinatal Medicine

DOI

10.3233/NPM-181854

Comments

Epub ahead of print

APA Citation

Kamalapathy, P., Fonda Allen, J. S., Macri, C. J., Lawrence, A. K., Regier, D. S., & Rubio, E. (2019). Whole-exome sequencing for diagnosis of Peters-plus syndrome after prenatal diagnosis of recurrent low PAPP-A and multiple fetal anomalies in two consecutive pregnancies.. Journal of Neonatal Perinatal Medicine, (). http://dx.doi.org/10.3233/NPM-181854

Peer Reviewed

1