APA

Gordon C. T., Chopra M., Oufadem M., Alibeu O., Bras M., Boddaert N., Bole-Feysot C., Nitschké P., Abadie V., Lyonnet S. & Amiel J. (20180621). MED13L loss-of-function variants in two patients with syndromic Pierre Robin sequence. : American journal of medical genetics. Part A.

Chicago

Gordon Christopher T, Chopra Maya, Oufadem Myriam, Alibeu Olivier, Bras Marc, Boddaert Nathalie, Bole-Feysot Christine, Nitschké Patrick, Abadie Véronique, Lyonnet Stanislas and Amiel Jeanne. 20180621. MED13L loss-of-function variants in two patients with syndromic Pierre Robin sequence. : American journal of medical genetics. Part A.

Harvard

Gordon C. T., Chopra M., Oufadem M., Alibeu O., Bras M., Boddaert N., Bole-Feysot C., Nitschké P., Abadie V., Lyonnet S. and Amiel J. (20180621). MED13L loss-of-function variants in two patients with syndromic Pierre Robin sequence. : American journal of medical genetics. Part A.

MLA

Gordon Christopher T, Chopra Maya, Oufadem Myriam, Alibeu Olivier, Bras Marc, Boddaert Nathalie, Bole-Feysot Christine, Nitschké Patrick, Abadie Véronique, Lyonnet Stanislas and Amiel Jeanne. MED13L loss-of-function variants in two patients with syndromic Pierre Robin sequence. : American journal of medical genetics. Part A. 20180621.