APA

Tsai E. A., Berman M. A., Conlin L. K., Rehm H. L., Francey L. J., Deardorff M. A., Holst J., Kaur M., Gallant E., Clark D. M., Glessner J. T., Jensen S. T., Grant S. F. A., Gruber P. J., Hakonarson H., Spinner N. B. & Krantz I. D. (20140326). PECONPI: a novel software for uncovering pathogenic copy number variations in non-syndromic sensorineural hearing loss and other genetically heterogeneous disorders. : American journal of medical genetics. Part A.

Chicago

Tsai Ellen A, Berman Micah A, Conlin Laura K, Rehm Heidi L, Francey Lauren J, Deardorff Matthew A, Holst Jenelle, Kaur Maninder, Gallant Emily, Clark Dinah M, Glessner Joseph T, Jensen Shane T, Grant Struan F A, Gruber Peter J, Hakonarson Hakon, Spinner Nancy B and Krantz Ian D. 20140326. PECONPI: a novel software for uncovering pathogenic copy number variations in non-syndromic sensorineural hearing loss and other genetically heterogeneous disorders. : American journal of medical genetics. Part A.

Harvard

Tsai E. A., Berman M. A., Conlin L. K., Rehm H. L., Francey L. J., Deardorff M. A., Holst J., Kaur M., Gallant E., Clark D. M., Glessner J. T., Jensen S. T., Grant S. F. A., Gruber P. J., Hakonarson H., Spinner N. B. and Krantz I. D. (20140326). PECONPI: a novel software for uncovering pathogenic copy number variations in non-syndromic sensorineural hearing loss and other genetically heterogeneous disorders. : American journal of medical genetics. Part A.

MLA

Tsai Ellen A, Berman Micah A, Conlin Laura K, Rehm Heidi L, Francey Lauren J, Deardorff Matthew A, Holst Jenelle, Kaur Maninder, Gallant Emily, Clark Dinah M, Glessner Joseph T, Jensen Shane T, Grant Struan F A, Gruber Peter J, Hakonarson Hakon, Spinner Nancy B and Krantz Ian D. PECONPI: a novel software for uncovering pathogenic copy number variations in non-syndromic sensorineural hearing loss and other genetically heterogeneous disorders. : American journal of medical genetics. Part A. 20140326.