22q11.2 deletion syndrome in diverse populations.

Authors

Paul Kruszka
Yonit A Addissie
Daniel E McGinn
Antonio R Porras
Elijah Biggs
Carlos R Ferreira, George Washington UniversityFollow
Marius George Linguraru, George Washington UniversityFollow
+several additional authors

Document Type

Journal Article

Publication Date

4-1-2017

Journal

American journal of medical genetics. Part A

Volume

173

Issue

4

Inclusive Pages

879-888

DOI

10.1002/ajmg.a.38199.

Keywords

Adolescent; Adult; African Continental Ancestry Group; Asian Continental Ancestry Group; Biometric Identification; Child; Child, Preschool; Chromosomes, Human, Pair 22; DiGeorge Syndrome; European Continental Ancestry Group; Facies; Female; Heart Defects, Congenital; Hispanic Americans; Humans; Image Interpretation, Computer-Assisted; In Situ Hybridization, Fluorescence; Infant; Infant, Newborn; Learning Disorders; Male; Phenotype

APA Citation

Kruszka, P., Addissie, Y., McGinn, D., Porras, A., Biggs, E., Ferreira, C., Linguraru, M., & +several additional authors (2017). 22q11.2 deletion syndrome in diverse populations.. American journal of medical genetics. Part A, 173 (4). http://dx.doi.org/10.1002/ajmg.a.38199.

Peer Reviewed

1