APA

Niceta M., Margiotti K., Digilio M. C., Guida V., Bruselles A., Pizzi S., Ferraris A., Memo L., Laforgia N., Dentici M. L., Consoli F., Torrente I., Ruiz-Perez V. L., Dallapiccola B., Marino B., De Luca A. & Tartaglia M. (20190911). Biallelic mutations in DYNC2LI1 are a rare cause of Ellis-van Creveld syndrome. : Clinical genetics.

Chicago

Niceta M, Margiotti K, Digilio M C, Guida V, Bruselles A, Pizzi S, Ferraris A, Memo L, Laforgia N, Dentici M L, Consoli F, Torrente I, Ruiz-Perez V L, Dallapiccola B, Marino B, De Luca A and Tartaglia M. 20190911. Biallelic mutations in DYNC2LI1 are a rare cause of Ellis-van Creveld syndrome. : Clinical genetics.

Harvard

Niceta M., Margiotti K., Digilio M. C., Guida V., Bruselles A., Pizzi S., Ferraris A., Memo L., Laforgia N., Dentici M. L., Consoli F., Torrente I., Ruiz-Perez V. L., Dallapiccola B., Marino B., De Luca A. and Tartaglia M. (20190911). Biallelic mutations in DYNC2LI1 are a rare cause of Ellis-van Creveld syndrome. : Clinical genetics.

MLA

Niceta M, Margiotti K, Digilio M C, Guida V, Bruselles A, Pizzi S, Ferraris A, Memo L, Laforgia N, Dentici M L, Consoli F, Torrente I, Ruiz-Perez V L, Dallapiccola B, Marino B, De Luca A and Tartaglia M. Biallelic mutations in DYNC2LI1 are a rare cause of Ellis-van Creveld syndrome. : Clinical genetics. 20190911.