APA
Al Turki S., Manickaraj A. K., Mercer C. L., Gerety S. S., Hitz M., Lindsay S., D'Alessandro L. C. A., Swaminathan G. J., Bentham J., Arndt A., Louw J., Breckpot J., Gewillig M., Thienpont B., Abdul-Khaliq H., Harnack C., Hoff K., Kramer H., Schubert S., Siebert R., Toka O., Cosgrove C., Watkins H., Lucassen A. M., O'Kelly I. M., Salmon A. P., Bu'Lock F. A., Granados-Riveron J., Setchfield K., Thornborough C., Brook J. D., Mulder B., Klaassen S., Bhattacharya S., Devriendt K., FitzPatrick D. R., Wilson D. I., Mital S. & Hurles M. E. (2016). Rare Variants in NR2F2 Cause Congenital Heart Defects in Humans. : American journal of human genetics.
Chicago
Al Turki Saeed, Manickaraj Ashok K, Mercer Catherine L, Gerety Sebastian S, Hitz Marc-Phillip, Lindsay Sarah, D'Alessandro Lisa C A, Swaminathan G Jawahar, Bentham Jamie, Arndt Anne-Karin, Louw Jacoba, Breckpot Jeroen, Gewillig Marc, Thienpont Bernard, Abdul-Khaliq Hashim, Harnack Christine, Hoff Kirstin, Kramer Hans-Heiner, Schubert Stephan, Siebert Reiner, Toka Okan, Cosgrove Catherine, Watkins Hugh, Lucassen Anneke M, O'Kelly Ita M, Salmon Anthony P, Bu'Lock Frances A, Granados-Riveron Javier, Setchfield Kerry, Thornborough Chris, Brook J David, Mulder Barbara, Klaassen Sabine, Bhattacharya Shoumo, Devriendt Koen, FitzPatrick David R, Wilson David I, Mital Seema and Hurles Matthew E. 2016. Rare Variants in NR2F2 Cause Congenital Heart Defects in Humans. : American journal of human genetics.
Harvard
Al Turki S., Manickaraj A. K., Mercer C. L., Gerety S. S., Hitz M., Lindsay S., D'Alessandro L. C. A., Swaminathan G. J., Bentham J., Arndt A., Louw J., Breckpot J., Gewillig M., Thienpont B., Abdul-Khaliq H., Harnack C., Hoff K., Kramer H., Schubert S., Siebert R., Toka O., Cosgrove C., Watkins H., Lucassen A. M., O'Kelly I. M., Salmon A. P., Bu'Lock F. A., Granados-Riveron J., Setchfield K., Thornborough C., Brook J. D., Mulder B., Klaassen S., Bhattacharya S., Devriendt K., FitzPatrick D. R., Wilson D. I., Mital S. and Hurles M. E. (2016). Rare Variants in NR2F2 Cause Congenital Heart Defects in Humans. : American journal of human genetics.
MLA
Al Turki Saeed, Manickaraj Ashok K, Mercer Catherine L, Gerety Sebastian S, Hitz Marc-Phillip, Lindsay Sarah, D'Alessandro Lisa C A, Swaminathan G Jawahar, Bentham Jamie, Arndt Anne-Karin, Louw Jacoba, Breckpot Jeroen, Gewillig Marc, Thienpont Bernard, Abdul-Khaliq Hashim, Harnack Christine, Hoff Kirstin, Kramer Hans-Heiner, Schubert Stephan, Siebert Reiner, Toka Okan, Cosgrove Catherine, Watkins Hugh, Lucassen Anneke M, O'Kelly Ita M, Salmon Anthony P, Bu'Lock Frances A, Granados-Riveron Javier, Setchfield Kerry, Thornborough Chris, Brook J David, Mulder Barbara, Klaassen Sabine, Bhattacharya Shoumo, Devriendt Koen, FitzPatrick David R, Wilson David I, Mital Seema and Hurles Matthew E. Rare Variants in NR2F2 Cause Congenital Heart Defects in Humans. : American journal of human genetics. 2016.