APA

Probst F. J., James R. A., Burrage L. C., Rosenfeld J. A., Bohan T. P., Ward Melver C. H., Magoulas P., Austin E., Franklin A. I. A., Azamian M., Xia F., Patel A., Bi W., Bacino C., Belmont J. W., Ware S. M., Shaw C., Cheung S. W. & Lalani S. R. (20160229). De novo deletions and duplications of 17q25.3 cause susceptibility to cardiovascular malformations. : Orphanet journal of rare diseases.

Chicago

Probst F J, James R A, Burrage L C, Rosenfeld J A, Bohan T P, Ward Melver C H, Magoulas P, Austin E, Franklin A I A, Azamian M, Xia F, Patel A, Bi W, Bacino C, Belmont J W, Ware S M, Shaw C, Cheung S W and Lalani S R. 20160229. De novo deletions and duplications of 17q25.3 cause susceptibility to cardiovascular malformations. : Orphanet journal of rare diseases.

Harvard

Probst F. J., James R. A., Burrage L. C., Rosenfeld J. A., Bohan T. P., Ward Melver C. H., Magoulas P., Austin E., Franklin A. I. A., Azamian M., Xia F., Patel A., Bi W., Bacino C., Belmont J. W., Ware S. M., Shaw C., Cheung S. W. and Lalani S. R. (20160229). De novo deletions and duplications of 17q25.3 cause susceptibility to cardiovascular malformations. : Orphanet journal of rare diseases.

MLA

Probst F J, James R A, Burrage L C, Rosenfeld J A, Bohan T P, Ward Melver C H, Magoulas P, Austin E, Franklin A I A, Azamian M, Xia F, Patel A, Bi W, Bacino C, Belmont J W, Ware S M, Shaw C, Cheung S W and Lalani S R. De novo deletions and duplications of 17q25.3 cause susceptibility to cardiovascular malformations. : Orphanet journal of rare diseases. 20160229.