APA

Grotto S., Drouin-Garraud V., Ounap K., Puusepp-Benazzouz H., Schuurs-Hoeijmakers J., Le Meur N., Chambon P., Fehrenbach S., van Bokhoven H., Frébourg T., de Brouwer A. P. M. & Saugier-Veber P. (20141209). Clinical assessment of five patients with BRWD3 mutation at Xq21.1 gives further evidence for mild to moderate intellectual disability and macrocephaly. : European journal of medical genetics.

Chicago

Grotto Sarah, Drouin-Garraud Valérie, Ounap Katrin, Puusepp-Benazzouz Helen, Schuurs-Hoeijmakers Janneke, Le Meur Nathalie, Chambon Pascal, Fehrenbach Séverine, van Bokhoven Hans, Frébourg Thierry, de Brouwer Arjan P M and Saugier-Veber Pascale. 20141209. Clinical assessment of five patients with BRWD3 mutation at Xq21.1 gives further evidence for mild to moderate intellectual disability and macrocephaly. : European journal of medical genetics.

Harvard

Grotto S., Drouin-Garraud V., Ounap K., Puusepp-Benazzouz H., Schuurs-Hoeijmakers J., Le Meur N., Chambon P., Fehrenbach S., van Bokhoven H., Frébourg T., de Brouwer A. P. M. and Saugier-Veber P. (20141209). Clinical assessment of five patients with BRWD3 mutation at Xq21.1 gives further evidence for mild to moderate intellectual disability and macrocephaly. : European journal of medical genetics.

MLA

Grotto Sarah, Drouin-Garraud Valérie, Ounap Katrin, Puusepp-Benazzouz Helen, Schuurs-Hoeijmakers Janneke, Le Meur Nathalie, Chambon Pascal, Fehrenbach Séverine, van Bokhoven Hans, Frébourg Thierry, de Brouwer Arjan P M and Saugier-Veber Pascale. Clinical assessment of five patients with BRWD3 mutation at Xq21.1 gives further evidence for mild to moderate intellectual disability and macrocephaly. : European journal of medical genetics. 20141209.