APA

Avila M., Dyment D. A., Sagen J. V., St-Onge J., Moog U., Chung B. H. Y., Mo S., Mansour S., Albanese A., Garcia S., Martin D. O., Lopez A. A., Claudi T., König R., White S. M., Sawyer S. L., Bernstein J. A., Slattery L., Jobling R. K., Yoon G., Curry C. J., Merrer M. L., Luyer B. L., Héron D., Mathieu-Dramard M., Bitoun P., Odent S., Amiel J., Kuentz P., Thevenon J., Laville M., Reznik Y., Fagour C., Nunes M., Delesalle D., Manouvrier S., Lascols O., Huet F., Binquet C., Faivre L., Rivière J., Vigouroux C., Njølstad P. R., Innes A. M. & Thauvin-Robinet C. (2016). Clinical reappraisal of SHORT syndrome with PIK3R1 mutations: toward recommendation for molecular testing and management. : Clinical genetics.

Chicago

Avila M, Dyment D A, Sagen J V, St-Onge J, Moog U, Chung B H Y, Mo S, Mansour S, Albanese A, Garcia S, Martin D O, Lopez A A, Claudi T, König R, White S M, Sawyer S L, Bernstein J A, Slattery L, Jobling R K, Yoon G, Curry C J, Merrer M L, Luyer B L, Héron D, Mathieu-Dramard M, Bitoun P, Odent S, Amiel J, Kuentz P, Thevenon J, Laville M, Reznik Y, Fagour C, Nunes M-L, Delesalle D, Manouvrier S, Lascols O, Huet F, Binquet C, Faivre L, Rivière J-B, Vigouroux C, Njølstad P R, Innes A M and Thauvin-Robinet C. 2016. Clinical reappraisal of SHORT syndrome with PIK3R1 mutations: toward recommendation for molecular testing and management. : Clinical genetics.

Harvard

Avila M., Dyment D. A., Sagen J. V., St-Onge J., Moog U., Chung B. H. Y., Mo S., Mansour S., Albanese A., Garcia S., Martin D. O., Lopez A. A., Claudi T., König R., White S. M., Sawyer S. L., Bernstein J. A., Slattery L., Jobling R. K., Yoon G., Curry C. J., Merrer M. L., Luyer B. L., Héron D., Mathieu-Dramard M., Bitoun P., Odent S., Amiel J., Kuentz P., Thevenon J., Laville M., Reznik Y., Fagour C., Nunes M., Delesalle D., Manouvrier S., Lascols O., Huet F., Binquet C., Faivre L., Rivière J., Vigouroux C., Njølstad P. R., Innes A. M. and Thauvin-Robinet C. (2016). Clinical reappraisal of SHORT syndrome with PIK3R1 mutations: toward recommendation for molecular testing and management. : Clinical genetics.

MLA

Avila M, Dyment D A, Sagen J V, St-Onge J, Moog U, Chung B H Y, Mo S, Mansour S, Albanese A, Garcia S, Martin D O, Lopez A A, Claudi T, König R, White S M, Sawyer S L, Bernstein J A, Slattery L, Jobling R K, Yoon G, Curry C J, Merrer M L, Luyer B L, Héron D, Mathieu-Dramard M, Bitoun P, Odent S, Amiel J, Kuentz P, Thevenon J, Laville M, Reznik Y, Fagour C, Nunes M-L, Delesalle D, Manouvrier S, Lascols O, Huet F, Binquet C, Faivre L, Rivière J-B, Vigouroux C, Njølstad P R, Innes A M and Thauvin-Robinet C. Clinical reappraisal of SHORT syndrome with PIK3R1 mutations: toward recommendation for molecular testing and management. : Clinical genetics. 2016.