Severe Nasomaxillary Hypoplasia (Binder phenotype) on Prenatal US/MRI: An Important Marker for the Prenatal Diagnosis of Chondrodysplasia Punctata.

Authors

Anna R Blask, George Washington University
Eva I Rubio, George Washington University
Kimberly A Chapman, George Washington University
Anne K Lawrence, George Washington University
Dorothy I Bulas, George Washington University

Document Type

Journal Article

Publication Date

7-1-2018

Journal

Pediatric radiology

Volume

48

Issue

7

Inclusive Pages

979-991

DOI

10.1007/s00247-018-4098-8

Keywords

Chondrodysplasia Punctata; Female; Gestational Age; Humans; Infant, Newborn; Magnetic Resonance Imaging; Maxilla; Nose; Phenotype; Pregnancy; Retrospective Studies; Ultrasonography, Prenatal

APA Citation

Blask, A., Rubio, E., Chapman, K., Lawrence, A., & Bulas, D. (2018). Severe Nasomaxillary Hypoplasia (Binder phenotype) on Prenatal US/MRI: An Important Marker for the Prenatal Diagnosis of Chondrodysplasia Punctata.. Pediatric radiology, 48 (7). http://dx.doi.org/10.1007/s00247-018-4098-8

Peer Reviewed

1