APA

Bacrot S., Mechler C., Talhi N., Martin-Coignard D., Roth P., Michot C., Ichkou A., Alibeu O., Nitschke P., Thomas S., Vekemans M., Razavi F., Boutaud L. & Attie-Bitach T. (20190318). Whole exome sequencing diagnoses the first fetal case of Bainbridge-Ropers syndrome presenting as pontocerebellar hypoplasia type 1. : Birth defects research.

Chicago

Bacrot Séverine, Mechler Charlotte, Talhi Naima, Martin-Coignard Dominique, Roth Philippe, Michot Caroline, Ichkou Amale, Alibeu Olivier, Nitschke Patrick, Thomas Sophie, Vekemans Michel, Razavi Férechté, Boutaud Lucile and Attie-Bitach Tania. 20190318. Whole exome sequencing diagnoses the first fetal case of Bainbridge-Ropers syndrome presenting as pontocerebellar hypoplasia type 1. : Birth defects research.

Harvard

Bacrot S., Mechler C., Talhi N., Martin-Coignard D., Roth P., Michot C., Ichkou A., Alibeu O., Nitschke P., Thomas S., Vekemans M., Razavi F., Boutaud L. and Attie-Bitach T. (20190318). Whole exome sequencing diagnoses the first fetal case of Bainbridge-Ropers syndrome presenting as pontocerebellar hypoplasia type 1. : Birth defects research.

MLA

Bacrot Séverine, Mechler Charlotte, Talhi Naima, Martin-Coignard Dominique, Roth Philippe, Michot Caroline, Ichkou Amale, Alibeu Olivier, Nitschke Patrick, Thomas Sophie, Vekemans Michel, Razavi Férechté, Boutaud Lucile and Attie-Bitach Tania. Whole exome sequencing diagnoses the first fetal case of Bainbridge-Ropers syndrome presenting as pontocerebellar hypoplasia type 1. : Birth defects research. 20190318.