APA

Radhakrishna U., Nath S. K., McElreavey K., Ratnamala U., Sun C., Maiti A. K., Gagnebin M., Béna F., Newkirk H. L., Sharp A. J., Everman D. B., Murray J. C., Schwartz C. E., Antonarakis S. E. & Butler M. G. (20120810). Genome-wide linkage and copy number variation analysis reveals 710 kb duplication on chromosome 1p31.3 responsible for autosomal dominant omphalocele. : Journal of medical genetics.

Chicago

Radhakrishna Uppala, Nath Swapan K, McElreavey Ken, Ratnamala Uppala, Sun Celi, Maiti Amit K, Gagnebin Maryline, Béna Frédérique, Newkirk Heather L, Sharp Andrew J, Everman David B, Murray Jeffrey C, Schwartz Charles E, Antonarakis Stylianos E and Butler Merlin G. 20120810. Genome-wide linkage and copy number variation analysis reveals 710 kb duplication on chromosome 1p31.3 responsible for autosomal dominant omphalocele. : Journal of medical genetics.

Harvard

Radhakrishna U., Nath S. K., McElreavey K., Ratnamala U., Sun C., Maiti A. K., Gagnebin M., Béna F., Newkirk H. L., Sharp A. J., Everman D. B., Murray J. C., Schwartz C. E., Antonarakis S. E. and Butler M. G. (20120810). Genome-wide linkage and copy number variation analysis reveals 710 kb duplication on chromosome 1p31.3 responsible for autosomal dominant omphalocele. : Journal of medical genetics.

MLA

Radhakrishna Uppala, Nath Swapan K, McElreavey Ken, Ratnamala Uppala, Sun Celi, Maiti Amit K, Gagnebin Maryline, Béna Frédérique, Newkirk Heather L, Sharp Andrew J, Everman David B, Murray Jeffrey C, Schwartz Charles E, Antonarakis Stylianos E and Butler Merlin G. Genome-wide linkage and copy number variation analysis reveals 710 kb duplication on chromosome 1p31.3 responsible for autosomal dominant omphalocele. : Journal of medical genetics. 20120810.