Source: Human Mutation. Unidades: HRACF, HRAC, IB
Subjects: DOENÇAS MUSCULOSQUELÉTICAS, ANORMALIDADES CRANIOFACIAIS, GENÉTICA
ABNT
VEGAS, Nancy; DEMIR, Zeynep; GORDON, Christopher T; et al. Further delineation of auriculocondylar syndrome based on 14 novel cases and reassessment of 25 published cases. Human Mutation, Hoboken, v. 43, n. 5, p. 582-594, 2022. Disponível em: < https://doi.org/10.1002/humu.24349 > DOI: 10.1002/humu.24349.APA
Vegas, N., Demir, Z., Gordon, C. T., Tavares, V. L. R., Zechi-Ceide, R. M., Kokitsu-Nakata, N. M., & Passos-Bueno, M. R. (2022). Further delineation of auriculocondylar syndrome based on 14 novel cases and reassessment of 25 published cases. Human Mutation, 43( 5), 582-594. doi:10.1002/humu.24349NLM
Vegas N, Demir Z, Gordon CT, Tavares VLR, Zechi-Ceide RM, Kokitsu-Nakata NM, Passos-Bueno MR. Further delineation of auriculocondylar syndrome based on 14 novel cases and reassessment of 25 published cases [Internet]. Human Mutation. 2022 ; 43( 5): 582-594.Available from: https://doi.org/10.1002/humu.24349Vancouver
Vegas N, Demir Z, Gordon CT, Tavares VLR, Zechi-Ceide RM, Kokitsu-Nakata NM, Passos-Bueno MR. Further delineation of auriculocondylar syndrome based on 14 novel cases and reassessment of 25 published cases [Internet]. Human Mutation. 2022 ; 43( 5): 582-594.Available from: https://doi.org/10.1002/humu.24349