Familial Axenfeld-Rieger anomaly, atrial septal defect, and sensorineural hearing loss: a possible new genetic syndrome.

MLA

Cunningham, E. T., Jr, et al. “Familial Axenfeld-Rieger Anomaly, Atrial Septal Defect, and Sensorineural Hearing Loss: A Possible New Genetic Syndrome.” Archives of Ophthalmology (Chicago, Ill. : 1960), vol. 116, no. 1, Jan. 1998, pp. 78–82. EBSCOhost, https://doi.org/10.1001/archopht.116.1.78.

APA

Cunningham, E. T., Jr, Eliott, D., Miller, N. R., Maumenee, I. H., & Green, W. R. (1998). Familial Axenfeld-Rieger anomaly, atrial septal defect, and sensorineural hearing loss: a possible new genetic syndrome. Archives of Ophthalmology (Chicago, Ill. : 1960), 116(1), 78–82. https://doi.org/10.1001/archopht.116.1.78

Chicago

Cunningham, E T, Jr, D Eliott, N R Miller, I H Maumenee, and W R Green. 1998. “Familial Axenfeld-Rieger Anomaly, Atrial Septal Defect, and Sensorineural Hearing Loss: A Possible New Genetic Syndrome.” Archives of Ophthalmology (Chicago, Ill. : 1960) 116 (1): 78–82. doi:10.1001/archopht.116.1.78.