Mutations in endothelin 1 cause auriculocondylar syndrome and isolated question mark ears (2014)
- Authors:
- Autor USP: CEIDE, ROSELI MARIA ZECHI - HRAC
- Unidade: HRAC
- Subjects: MUTAÇÃO GENÉTICA; MALFORMAÇÕES; DOENÇAS GENÉTICAS
- Language: Inglês
- Imprenta:
- Source:
- Título do periódico: Abstracts
- Conference titles: European Human Genetics Conference
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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: 23 abr. 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 abr. 23 ] -
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 abr. 23 ] - Baraitser-Winter cerebrofrontofacial syndrome: delineation of the spectrum in 42 cases
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