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Filtros : "Bélgica" "Passos-Bueno, Maria Rita" Removidos: "FCF025" "QFL" "1930" Limpar

Filtros

USP affiliated authors
- bueno, maria rita dos santos e passos (~2)
- ceide, roseli maria zechi (~1)
- nakata, nancy mizue kokitsu (~1)
- tavares, vanessa luiza romanelli (~1)
Date published
- 2022 (~1)
- 2018 (~1)
Subjects
- anomalia craniofacial (1)
- anormalidades craniofaciais (1)
- dente (1)
- doenças musculosqueléticas (1)
- genética (1)

Collaboration
Normalized affiliation
Non normalized affiliation
- chu lille, clinique de génétique guy fontaine, lille (1)
- center for human genetics, cliniques universitaires saint luc, université catholique de louvain, brussels (1)
- centre de génétique-centre de référence des maladies rares, anomalies du développement et syndrome malformatifs, centre hospitalo-universitaire de dijon, bourgogne (1)
- department of biomolecular medicine, center for medical genetics, ghent university hospital, ghent university, ghent (1)
- department of genetics, sultan qaboos university hospital, muscat (1)

Countries of institutions of collaboration
- bélgica (2)
- inglaterra (2)
- austrália (1)
- canadá (1)
- dinamarca (1)

Artigo de periodico
Further delineation of auriculocondylar syndrome based on 14 novel cases and reassessment of 25 published cases (2022)
Vegas, Nancy ; Demir, Zeynep; Gordon, Christopher T.; Breton, Sylvain; Tavares, Vanessa Luiza Romanelli ; Moisset, Hugo; Zechi-Ceide, Roseli Maria ; Kokitsu-Nakata, Nancy M.; Kido, Yasuhiro; Marlin, Sandrine; Halem, Souad Gherbi; Meerschaut, Ilse; Callewaert, Bert; Chung, Brian ; Revencu, Nicole; Lehalle, Daphné; Petit, Florence ; Propst, Evan J.; Papsin, Blake C.; Phillips, John H.; Jakobsen, Linda; Tanno, Pauline Le; Thévenon, Julien; McGaughran, Julie; Gerkes, Erica H.; Leoni, Chiara; Kroisel, Peter; Tan, Tiong Y.; Henderson, Alex; Terhal, Paulien; Basel-Salmon, Lina; Alkindy, Adila; White, Susan M.; Passos-Bueno, Maria Rita ; Pingault, Véronique; Pontual, Loïc De; Amiel, Jeanne
Source: Human Mutation. Unidades: HRACF, HRAC, IB
Subjects: DOENÇAS MUSCULOSQUELÉTICAS, ANORMALIDADES CRANIOFACIAIS, GENÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
VEGAS, Nancy et al. Further delineation of auriculocondylar syndrome based on 14 novel cases and reassessment of 25 published cases. Human Mutation, v. 43, n. 5, p. 582-594, 2022Tradução . . Disponível em: https://doi.org/10.1002/humu.24349. Acesso em: 03 nov. 2024.
APA
Vegas, N., Demir, Z., Gordon, C. T., Breton, S., Tavares, V. L. R., Moisset, H., et al. (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.24349
NLM
Vegas N, Demir Z, Gordon CT, Breton S, Tavares VLR, Moisset H, Zechi-Ceide RM, Kokitsu-Nakata NM, Kido Y, Marlin S, Halem SG, Meerschaut I, Callewaert B, Chung B, Revencu N, Lehalle D, Petit F, Propst EJ, Papsin BC, Phillips JH, Jakobsen L, Tanno PL, Thévenon J, McGaughran J, Gerkes EH, Leoni C, Kroisel P, Tan TY, Henderson A, Terhal P, Basel-Salmon L, Alkindy A, White SM, Passos-Bueno MR, Pingault V, Pontual LD, Amiel J. Further delineation of auriculocondylar syndrome based on 14 novel cases and reassessment of 25 published cases [Internet]. Human Mutation. 2022 ; 43( 5): 582-594.[citado 2024 nov. 03 ] Available from: https://doi.org/10.1002/humu.24349
Vancouver
Vegas N, Demir Z, Gordon CT, Breton S, Tavares VLR, Moisset H, Zechi-Ceide RM, Kokitsu-Nakata NM, Kido Y, Marlin S, Halem SG, Meerschaut I, Callewaert B, Chung B, Revencu N, Lehalle D, Petit F, Propst EJ, Papsin BC, Phillips JH, Jakobsen L, Tanno PL, Thévenon J, McGaughran J, Gerkes EH, Leoni C, Kroisel P, Tan TY, Henderson A, Terhal P, Basel-Salmon L, Alkindy A, White SM, Passos-Bueno MR, Pingault V, Pontual LD, Amiel J. Further delineation of auriculocondylar syndrome based on 14 novel cases and reassessment of 25 published cases [Internet]. Human Mutation. 2022 ; 43( 5): 582-594.[citado 2024 nov. 03 ] Available from: https://doi.org/10.1002/humu.24349
Artigo de periodico
Zebrafish sp7 mutants show tooth cycling independent of attachment, eruption and poor differentiation of teeth (2018)
Kague, E; Witten, P. E; Soenens, M; Campos, C. L; Lubiana, T; Fisher, S; Hammond, C; Robson Brown, K; Passos-Bueno, Maria Rita ; Huysseune, A
Source: Developmental Biology. Unidade: IB
Subjects: ANOMALIA CRANIOFACIAL, MALFORMAÇÕES, ODONTOGÊNESE, GENÉTICA MOLECULAR, MODELOS ANIMAIS, DENTE
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
KAGUE, E et al. Zebrafish sp7 mutants show tooth cycling independent of attachment, eruption and poor differentiation of teeth. Developmental Biology, v. 435, n. 2, p. 176-184, 2018Tradução . . Disponível em: https://doi.org/10.1016/j.ydbio.2018.01.021. Acesso em: 03 nov. 2024.
APA
Kague, E., Witten, P. E., Soenens, M., Campos, C. L., Lubiana, T., Fisher, S., et al. (2018). Zebrafish sp7 mutants show tooth cycling independent of attachment, eruption and poor differentiation of teeth. Developmental Biology, 435( 2), 176-184. doi:10.1016/j.ydbio.2018.01.021
NLM
Kague E, Witten PE, Soenens M, Campos CL, Lubiana T, Fisher S, Hammond C, Robson Brown K, Passos-Bueno MR, Huysseune A. Zebrafish sp7 mutants show tooth cycling independent of attachment, eruption and poor differentiation of teeth [Internet]. Developmental Biology. 2018 ; 435( 2): 176-184.[citado 2024 nov. 03 ] Available from: https://doi.org/10.1016/j.ydbio.2018.01.021
Vancouver
Kague E, Witten PE, Soenens M, Campos CL, Lubiana T, Fisher S, Hammond C, Robson Brown K, Passos-Bueno MR, Huysseune A. Zebrafish sp7 mutants show tooth cycling independent of attachment, eruption and poor differentiation of teeth [Internet]. Developmental Biology. 2018 ; 435( 2): 176-184.[citado 2024 nov. 03 ] Available from: https://doi.org/10.1016/j.ydbio.2018.01.021

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