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Artigo de periodico
Mutations in the endothelin receptor type A cause mandibulofacial dysostosis with alopecia (2015)
Gordon, Christopher T; Weaver, K. Nicole; Zechi-Ceide, Roseli Maria ; Madsen, Erik C.; Tavares, Andre L. P.; Oufadem, Myriam; Kurihara, Yukiko; Adameyko, Igor; Picard, Arnaud ; Breton, Sylvain; Pierrot, Sébastien; Biosse-Duplan, Martin; Voisin, Norine; Masson, Cécile; Bole-Feysot, Christine; Nitschké, Patrick; Delrue, Marie-Ange; Lacombe, Didier; Guion-Almeida, Maria Leine; Moura, Priscila Padilha; Garib, Daniela Gamba ; Munnich, Arnold; Ernfors, Patrik; Hufnagel, Robert B.; Hopkin, Robert J.
Source: American Journal of Human Genetics. Unidades: HRAC, FOB
Subjects: ALOPECIA, DISOSTOSE MANDIBULOFACIAL, MUTAÇÃO GENÉTICA, TOMOGRAFIA COMPUTADORIZADA POR RAIOS X
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
GORDON, Christopher T et al. Mutations in the endothelin receptor type A cause mandibulofacial dysostosis with alopecia. American Journal of Human Genetics, v. 96, n. 4, p. 519-531, 2015Tradução . . Disponível em: https://doi.org/10.1016/j.ajhg.2015.01.015. Acesso em: 05 nov. 2024.
APA
Gordon, C. T., Weaver, K. N., Zechi-Ceide, R. M., Madsen, E. C., Tavares, A. L. P., Oufadem, M., et al. (2015). Mutations in the endothelin receptor type A cause mandibulofacial dysostosis with alopecia. American Journal of Human Genetics, 96( 4), 519-531. doi:10.1016/j.ajhg.2015.01.015
NLM
Gordon CT, Weaver KN, Zechi-Ceide RM, Madsen EC, Tavares ALP, Oufadem M, Kurihara Y, Adameyko I, Picard A, Breton S, Pierrot S, Biosse-Duplan M, Voisin N, Masson C, Bole-Feysot C, Nitschké P, Delrue M-A, Lacombe D, Guion-Almeida ML, Moura PP, Garib DG, Munnich A, Ernfors P, Hufnagel RB, Hopkin RJ. Mutations in the endothelin receptor type A cause mandibulofacial dysostosis with alopecia [Internet]. American Journal of Human Genetics. 2015 ; 96( 4): 519-531.[citado 2024 nov. 05 ] Available from: https://doi.org/10.1016/j.ajhg.2015.01.015
Vancouver
Gordon CT, Weaver KN, Zechi-Ceide RM, Madsen EC, Tavares ALP, Oufadem M, Kurihara Y, Adameyko I, Picard A, Breton S, Pierrot S, Biosse-Duplan M, Voisin N, Masson C, Bole-Feysot C, Nitschké P, Delrue M-A, Lacombe D, Guion-Almeida ML, Moura PP, Garib DG, Munnich A, Ernfors P, Hufnagel RB, Hopkin RJ. Mutations in the endothelin receptor type A cause mandibulofacial dysostosis with alopecia [Internet]. American Journal of Human Genetics. 2015 ; 96( 4): 519-531.[citado 2024 nov. 05 ] Available from: https://doi.org/10.1016/j.ajhg.2015.01.015
Trabalho de evento-resumo
Mutations in endothelin 1 cause auriculocondylar syndrome and isolated question mark ears (2014)
Gordon, Christhofer T.; Petit, Florence; Kroisel, P.; Jakobsen, Linda; Ceide, Roseli Maria Zechi; Oufadem, Myriam; Bole-Feysot, C.; Nitschke, Patrick; Munnich, Arnold; Lyonnet, Stanislas; Holder-Espinasse, M.; Amiel, Jeanne
Source: Abstracts. Conference titles: European Human Genetics Conference. Unidade: HRAC
Subjects: MUTAÇÃO GENÉTICA, MALFORMAÇÕES, DOENÇAS GENÉTICAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
GORDON, Christhofer T. et al. Mutations in endothelin 1 cause auriculocondylar syndrome and isolated question mark ears. 2014, Anais.. Milan: ESHG, 2014. . Acesso em: 05 nov. 2024.
APA
Gordon, C. T., Petit, F., Kroisel, P., Jakobsen, L., Ceide, R. M. Z., Oufadem, M., et al. (2014). Mutations in endothelin 1 cause auriculocondylar syndrome and isolated question mark ears. In Abstracts. Milan: ESHG.
NLM
Gordon CT, Petit F, Kroisel P, Jakobsen L, Ceide RMZ, Oufadem M, Bole-Feysot C, Nitschke P, Munnich A, Lyonnet S, Holder-Espinasse M, Amiel J. Mutations in endothelin 1 cause auriculocondylar syndrome and isolated question mark ears. Abstracts. 2014 ;[citado 2024 nov. 05 ]
Vancouver
Gordon CT, Petit F, Kroisel P, Jakobsen L, Ceide RMZ, Oufadem M, Bole-Feysot C, Nitschke P, Munnich A, Lyonnet S, Holder-Espinasse M, Amiel J. Mutations in endothelin 1 cause auriculocondylar syndrome and isolated question mark ears. Abstracts. 2014 ;[citado 2024 nov. 05 ]
Artigo de periodico
Mutations in endothelin 1 cause recessive auriculocondylar syndrome and dominant isolated question-mark ears (2013)
Gordon, Christopher J; Petit, Florence; Kroisel, Peter Michael; Jakobsen, Linda; Zechi-Ceide, Roseli Maria ; Oufadem, Myriam; Bole-Feysot, C; Pruvost, Solenn; Masson, Cécile; Tores, Frédéric; Hieu, Thierry; Nitschké, Patrick; Lindholm, Pernille; Pellerin, Philippe; Guion-Almeida, Maria Leine; Nakata, Nancy Mizue Kokitsu ; Pittoli, Siulan Vendramini Paulovich ; Munnich, Arnold; Lyonnet, Stanislas; Holder-Espinasse, Muriel; Amiel, Jeanne
Source: American Journal of Human Genetics. Unidade: HRAC
Subjects: OTOPATIAS, FENÓTIPOS, ENDOTELINAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
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: 05 nov. 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.2013.10.023
NLM
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 nov. 05 ] Available from: https://doi.org/10.1016/j.ajhg.2013.10.023
Vancouver
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 nov. 05 ] Available from: https://doi.org/10.1016/j.ajhg.2013.10.023

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