Xq22.3q23 microdeletion harboring TMEM164 and AMMECR1 genes: Two case reports confirming a recognizable phenotype with short stature, midface hypoplasia, intellectual delay, and elliptocytosis

MLA

Renaud Touraine, et al. “Xq22.3q23 Microdeletion Harboring TMEM164 and AMMECR1 Genes: Two Case Reports Confirming a Recognizable Phenotype with Short Stature, Midface Hypoplasia, Intellectual Delay, and Elliptocytosis.” American Journal of Medical Genetics Part A, vol. 179, Feb. 2019, pp. 650–54. EBSCOhost, https://doi.org/10.1002/ajmg.a.61057.

APA

Renaud Touraine, Véronique Adouard, Pierre-Simon Jouk, Véronique Satre, Radu Harbuz, Claire Vettier, Claire Barro, Charles Coutton, Francis Ramond, Julien Thevenon, Brice Poreau, & Klaus Dieterich. (2019). Xq22.3q23 microdeletion harboring TMEM164 and AMMECR1 genes: Two case reports confirming a recognizable phenotype with short stature, midface hypoplasia, intellectual delay, and elliptocytosis. American Journal of Medical Genetics Part A, 179, 650–654. https://doi.org/10.1002/ajmg.a.61057

Chicago

Renaud Touraine, Véronique Adouard, Pierre-Simon Jouk, Véronique Satre, Radu Harbuz, Claire Vettier, Claire Barro, et al. 2019. “Xq22.3q23 Microdeletion Harboring TMEM164 and AMMECR1 Genes: Two Case Reports Confirming a Recognizable Phenotype with Short Stature, Midface Hypoplasia, Intellectual Delay, and Elliptocytosis.” American Journal of Medical Genetics Part A 179 (February): 650–54. doi:10.1002/ajmg.a.61057.