APA (7th ed.) Citation

(18281710), A. K., (18281713), L. H., (18281716), C. T., (295984), G. N., & (122847), M. K. (2022). A novel pathogenic <i>CDH3</i> variant underlying heredity hypotrichosis simplex detected by whole-exome sequencing (WES)—a case report.

Chicago Style (17th ed.) Citation

(18281710), Ayat Kadhi, Lamiaa Hamie (18281713), Christel Tamer (18281716), Georges Nemer (295984), and Mazen Kurban (122847). A Novel Pathogenic <i>CDH3</i> Variant Underlying Heredity Hypotrichosis Simplex Detected by Whole-exome Sequencing (WES)—a Case Report. 2022.

MLA (9th ed.) Citation

(18281710), Ayat Kadhi, et al. A Novel Pathogenic <i>CDH3</i> Variant Underlying Heredity Hypotrichosis Simplex Detected by Whole-exome Sequencing (WES)—a Case Report. 2022.