Source: American Journal of Human Genetics. Unidade: HRAC
Subjects: OTOPATIAS, FENÓTIPOS, ENDOTELINAS
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GORDON, Christopher J et al. Mutations in endothelin 1 cause recessive auriculocondylar syndrome and dominant isolated question-mark ears. American Journal of Human Genetics, v. 93, n. 6, p. 1118-1125, 2013Tradução . . Disponível em: https://doi.org/10.1016/j.ajhg.2013.10.023. Acesso em: 15 out. 2024.APA
Gordon, C. J., Petit, F., Kroisel, P. M., Jakobsen, L., Zechi-Ceide, R. M., Oufadem, M., et al. (2013). Mutations in endothelin 1 cause recessive auriculocondylar syndrome and dominant isolated question-mark ears. American Journal of Human Genetics, 93( 6), 1118-1125. doi:10.1016/j.ajhg.2013.10.023NLM
Gordon CJ, Petit F, Kroisel PM, Jakobsen L, Zechi-Ceide RM, Oufadem M, Bole-Feysot C, Pruvost S, Masson C, Tores F, Hieu T, Nitschké P, Lindholm P, Pellerin P, Guion-Almeida ML, Nakata NMK, Pittoli SVP, Munnich A, Lyonnet S, Holder-Espinasse M, Amiel J. Mutations in endothelin 1 cause recessive auriculocondylar syndrome and dominant isolated question-mark ears [Internet]. American Journal of Human Genetics. 2013 ; 93( 6): 1118-1125.[citado 2024 out. 15 ] Available from: https://doi.org/10.1016/j.ajhg.2013.10.023Vancouver
Gordon CJ, Petit F, Kroisel PM, Jakobsen L, Zechi-Ceide RM, Oufadem M, Bole-Feysot C, Pruvost S, Masson C, Tores F, Hieu T, Nitschké P, Lindholm P, Pellerin P, Guion-Almeida ML, Nakata NMK, Pittoli SVP, Munnich A, Lyonnet S, Holder-Espinasse M, Amiel J. Mutations in endothelin 1 cause recessive auriculocondylar syndrome and dominant isolated question-mark ears [Internet]. American Journal of Human Genetics. 2013 ; 93( 6): 1118-1125.[citado 2024 out. 15 ] Available from: https://doi.org/10.1016/j.ajhg.2013.10.023