APA
Gordon C. T., Petit F., Kroisel P. M., Jakobsen L., Zechi-Ceide R. M., Oufadem M., Bole-Feysot C., Pruvost S., Masson C., Tores F., Hieu T., Nitschké P., Lindholm P., Pellerin P., Guion-Almeida M. L., Kokitsu-Nakata N. M., Vendramini-Pittoli S., Munnich A., Lyonnet S., Holder-Espinasse M. & Amiel J. (20140212). Mutations in endothelin 1 cause recessive auriculocondylar syndrome and dominant isolated question-mark ears. : American journal of human genetics.
Chicago
Gordon Christopher T, Petit Florence, Kroisel Peter M, Jakobsen Linda, Zechi-Ceide Roseli Maria, Oufadem Myriam, Bole-Feysot Christine, Pruvost Solenn, Masson Cécile, Tores Frédéric, Hieu Thierry, Nitschké Patrick, Lindholm Pernille, Pellerin Philippe, Guion-Almeida Maria Leine, Kokitsu-Nakata Nancy Mizue, Vendramini-Pittoli Siulan, Munnich Arnold, Lyonnet Stanislas, Holder-Espinasse Muriel and Amiel Jeanne. 20140212. Mutations in endothelin 1 cause recessive auriculocondylar syndrome and dominant isolated question-mark ears. : American journal of human genetics.
Harvard
Gordon C. T., Petit F., Kroisel P. M., Jakobsen L., Zechi-Ceide R. M., Oufadem M., Bole-Feysot C., Pruvost S., Masson C., Tores F., Hieu T., Nitschké P., Lindholm P., Pellerin P., Guion-Almeida M. L., Kokitsu-Nakata N. M., Vendramini-Pittoli S., Munnich A., Lyonnet S., Holder-Espinasse M. and Amiel J. (20140212). Mutations in endothelin 1 cause recessive auriculocondylar syndrome and dominant isolated question-mark ears. : American journal of human genetics.
MLA
Gordon Christopher T, Petit Florence, Kroisel Peter M, Jakobsen Linda, Zechi-Ceide Roseli Maria, Oufadem Myriam, Bole-Feysot Christine, Pruvost Solenn, Masson Cécile, Tores Frédéric, Hieu Thierry, Nitschké Patrick, Lindholm Pernille, Pellerin Philippe, Guion-Almeida Maria Leine, Kokitsu-Nakata Nancy Mizue, Vendramini-Pittoli Siulan, Munnich Arnold, Lyonnet Stanislas, Holder-Espinasse Muriel and Amiel Jeanne. Mutations in endothelin 1 cause recessive auriculocondylar syndrome and dominant isolated question-mark ears. : American journal of human genetics. 20140212.