APA

Breckpot J., Tranchevent L., Thienpont B., Bauters M., Troost E., Gewillig M., Vermeesch J. R., Moreau Y., Devriendt K. & Van Esch H. (20120605). BMPR1A is a candidate gene for congenital heart defects associated with the recurrent 10q22q23 deletion syndrome. : European journal of medical genetics.

Chicago

Breckpot Jeroen, Tranchevent Léon-Charles, Thienpont Bernard, Bauters Marijke, Troost Els, Gewillig Marc, Vermeesch Joris R, Moreau Yves, Devriendt Koenraad and Van Esch Hilde. 20120605. BMPR1A is a candidate gene for congenital heart defects associated with the recurrent 10q22q23 deletion syndrome. : European journal of medical genetics.

Harvard

Breckpot J., Tranchevent L., Thienpont B., Bauters M., Troost E., Gewillig M., Vermeesch J. R., Moreau Y., Devriendt K. and Van Esch H. (20120605). BMPR1A is a candidate gene for congenital heart defects associated with the recurrent 10q22q23 deletion syndrome. : European journal of medical genetics.

MLA

Breckpot Jeroen, Tranchevent Léon-Charles, Thienpont Bernard, Bauters Marijke, Troost Els, Gewillig Marc, Vermeesch Joris R, Moreau Yves, Devriendt Koenraad and Van Esch Hilde. BMPR1A is a candidate gene for congenital heart defects associated with the recurrent 10q22q23 deletion syndrome. : European journal of medical genetics. 20120605.