APA

Chassaing N., De Mas P., Tauber M., Vincent M. C., Julia S., Bourrouillou G., Calvas P. & Bieth E. (20050218). Molecular characterization of a cryptic 2q37 deletion in a patient with Albright hereditary osteodystrophy-like phenotype. : American journal of medical genetics. Part A.

Chicago

Chassaing N, De Mas P, Tauber M, Vincent M C, Julia S, Bourrouillou G, Calvas P and Bieth E. 20050218. Molecular characterization of a cryptic 2q37 deletion in a patient with Albright hereditary osteodystrophy-like phenotype. : American journal of medical genetics. Part A.

Harvard

Chassaing N., De Mas P., Tauber M., Vincent M. C., Julia S., Bourrouillou G., Calvas P. and Bieth E. (20050218). Molecular characterization of a cryptic 2q37 deletion in a patient with Albright hereditary osteodystrophy-like phenotype. : American journal of medical genetics. Part A.

MLA

Chassaing N, De Mas P, Tauber M, Vincent M C, Julia S, Bourrouillou G, Calvas P and Bieth E. Molecular characterization of a cryptic 2q37 deletion in a patient with Albright hereditary osteodystrophy-like phenotype. : American journal of medical genetics. Part A. 20050218.