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Artigo de periodico
Cephalometric findings in nine individuals with Richieri-Costa-Pereira syndrome (2018)
Pinto, Rayane de Oliveira; Peixoto, Adriano Porto; Pinto, Ary dos Santos; Richieri-Costa, Antonio; Ceide, Roseli Maria Zechi; Ozawa, Terumi Okada; Dalben, Gisele da Silva
Source: The Journal of Craniofacial Surgery. Unidades: HRAC, HRACF
Subjects: ANORMALIDADES CRANIOFACIAIS, MICROGNATISMO, DISOSTOSE CRÂNIOFACIAL, ANORMALIDADES MÚLTIPLAS
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ABNT
PINTO, Rayane de Oliveira et al. Cephalometric findings in nine individuals with Richieri-Costa-Pereira syndrome. The Journal of Craniofacial Surgery, v. 29, n. 6, p. 1596-1600, 2018Tradução . . Disponível em: https://doi.org/10.1097/SCS.0000000000004588. Acesso em: 12 nov. 2024.
APA
Pinto, R. de O., Peixoto, A. P., Pinto, A. dos S., Richieri-Costa, A., Ceide, R. M. Z., Ozawa, T. O., & Dalben, G. da S. (2018). Cephalometric findings in nine individuals with Richieri-Costa-Pereira syndrome. The Journal of Craniofacial Surgery, 29( 6), 1596-1600. doi:10.1097/SCS.0000000000004588
NLM
Pinto R de O, Peixoto AP, Pinto A dos S, Richieri-Costa A, Ceide RMZ, Ozawa TO, Dalben G da S. Cephalometric findings in nine individuals with Richieri-Costa-Pereira syndrome [Internet]. The Journal of Craniofacial Surgery. 2018 ; 29( 6): 1596-1600.[citado 2024 nov. 12 ] Available from: https://doi.org/10.1097/SCS.0000000000004588
Vancouver
Pinto R de O, Peixoto AP, Pinto A dos S, Richieri-Costa A, Ceide RMZ, Ozawa TO, Dalben G da S. Cephalometric findings in nine individuals with Richieri-Costa-Pereira syndrome [Internet]. The Journal of Craniofacial Surgery. 2018 ; 29( 6): 1596-1600.[citado 2024 nov. 12 ] Available from: https://doi.org/10.1097/SCS.0000000000004588
Artigo de periodico
Deficiency of the cytoskeletal protein SPECC1L leads to oblique facial clefting (2011)
Saadi, Irfan; Alkuraya, Fowzan S.; Gisselbrecht, Stephen S.; Goessling, Wolfram; Cavallesco, Resy; Turbe-Doan, Annick; Petrin, Aline L; Harris, James; Siddiqui, Ursela; Grix Junior, Arthur W.; Hove, Hanne D.; Leboulch, Philippe; Glover, Thomas W.; Morton, Cynthia C; Richieri-Costa, Antonio ; Murray, Jeffrey C; Erickson, Robert P.; Maas, Richard L.
Source: American Journal of Human Genetics. Unidade: HRAC
Subjects: DEFICIÊNCIA DE PROTEÍNA, ANORMALIDADES CRANIOFACIAIS, FENÓTIPOS, DISOSTOSE CRÂNIOFACIAL, FISSURA PALATINA
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ABNT
SAADI, Irfan et al. Deficiency of the cytoskeletal protein SPECC1L leads to oblique facial clefting. American Journal of Human Genetics, v. 89, p. 44-55, 2011Tradução . . Disponível em: https://doi.org/10.1016/j.ajhg.2011.05.023. Acesso em: 12 nov. 2024.
APA
Saadi, I., Alkuraya, F. S., Gisselbrecht, S. S., Goessling, W., Cavallesco, R., Turbe-Doan, A., et al. (2011). Deficiency of the cytoskeletal protein SPECC1L leads to oblique facial clefting. American Journal of Human Genetics, 89, 44-55. doi:10.1016/j.ajhg.2011.05.023
NLM
Saadi I, Alkuraya FS, Gisselbrecht SS, Goessling W, Cavallesco R, Turbe-Doan A, Petrin AL, Harris J, Siddiqui U, Grix Junior AW, Hove HD, Leboulch P, Glover TW, Morton CC, Richieri-Costa A, Murray JC, Erickson RP, Maas RL. Deficiency of the cytoskeletal protein SPECC1L leads to oblique facial clefting [Internet]. American Journal of Human Genetics. 2011 ; 89 44-55.[citado 2024 nov. 12 ] Available from: https://doi.org/10.1016/j.ajhg.2011.05.023
Vancouver
Saadi I, Alkuraya FS, Gisselbrecht SS, Goessling W, Cavallesco R, Turbe-Doan A, Petrin AL, Harris J, Siddiqui U, Grix Junior AW, Hove HD, Leboulch P, Glover TW, Morton CC, Richieri-Costa A, Murray JC, Erickson RP, Maas RL. Deficiency of the cytoskeletal protein SPECC1L leads to oblique facial clefting [Internet]. American Journal of Human Genetics. 2011 ; 89 44-55.[citado 2024 nov. 12 ] Available from: https://doi.org/10.1016/j.ajhg.2011.05.023
Trabalho de evento-resumo
Robin sequence with cleft mandible and limb anomalies: a brazilian founder condition or an extremely rare syndrome? (2009)
Favaro, F P; Zechi-Ceide, Roseli Maria ; Maximino, Luciana Paula ; Antunes, L F P P; Richieri-Costa, Antonio ; Guion-Almeida, Maria Leine
Source: Anais. Conference titles: Simpósio Internacional de Fissuras Orofaciais e Anomalias Relacionadas. Unidades: HRACF, FOB, HRAC
Subjects: SÍNDROME DE PIERRE ROBIN, FISSURA LÁBIOPALATINA, DISOSTOSE CRÂNIOFACIAL
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ABNT
FAVARO, F P et al. Robin sequence with cleft mandible and limb anomalies: a brazilian founder condition or an extremely rare syndrome? 2009, Anais.. Bauru: Universidade de São Paulo, Hospital de Reabilitação de Anomalias Craniofaciais, 2009. Disponível em: https://repositorio.usp.br/directbitstream/045a13cd-5fcd-41c2-9a71-a6a5fd50d0fc/3209302.pdf. Acesso em: 12 nov. 2024.
APA
Favaro, F. P., Zechi-Ceide, R. M., Maximino, L. P., Antunes, L. F. P. P., Richieri-Costa, A., & Guion-Almeida, M. L. (2009). Robin sequence with cleft mandible and limb anomalies: a brazilian founder condition or an extremely rare syndrome? In Anais. Bauru: Universidade de São Paulo, Hospital de Reabilitação de Anomalias Craniofaciais. Recuperado de https://repositorio.usp.br/directbitstream/045a13cd-5fcd-41c2-9a71-a6a5fd50d0fc/3209302.pdf
NLM
Favaro FP, Zechi-Ceide RM, Maximino LP, Antunes LFPP, Richieri-Costa A, Guion-Almeida ML. Robin sequence with cleft mandible and limb anomalies: a brazilian founder condition or an extremely rare syndrome? [Internet]. Anais. 2009 ;[citado 2024 nov. 12 ] Available from: https://repositorio.usp.br/directbitstream/045a13cd-5fcd-41c2-9a71-a6a5fd50d0fc/3209302.pdf
Vancouver
Favaro FP, Zechi-Ceide RM, Maximino LP, Antunes LFPP, Richieri-Costa A, Guion-Almeida ML. Robin sequence with cleft mandible and limb anomalies: a brazilian founder condition or an extremely rare syndrome? [Internet]. Anais. 2009 ;[citado 2024 nov. 12 ] Available from: https://repositorio.usp.br/directbitstream/045a13cd-5fcd-41c2-9a71-a6a5fd50d0fc/3209302.pdf
Artigo de periodico
Acrofrontofacionasal dysostosis: report of the third Brazilian family (2003)
Guion-Almeida, Maria Leine; Richieri-Costa, Antonio
Source: American Journal of Medical Genetics. Unidade: HRAC
Assunto: DISOSTOSE CRÂNIOFACIAL
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ABNT
GUION-ALMEIDA, Maria Leine e RICHIERI-COSTA, Antonio. Acrofrontofacionasal dysostosis: report of the third Brazilian family. American Journal of Medical Genetics, v. 119A, n. 2, p. 238-241, 2003Tradução . . Disponível em: https://doi.org/10.1002/ajmg.a.10444. Acesso em: 12 nov. 2024.
APA
Guion-Almeida, M. L., & Richieri-Costa, A. (2003). Acrofrontofacionasal dysostosis: report of the third Brazilian family. American Journal of Medical Genetics, 119A( 2), 238-241. doi:10.1002/ajmg.a.10444
NLM
Guion-Almeida ML, Richieri-Costa A. Acrofrontofacionasal dysostosis: report of the third Brazilian family [Internet]. American Journal of Medical Genetics. 2003 ; 119A( 2): 238-241.[citado 2024 nov. 12 ] Available from: https://doi.org/10.1002/ajmg.a.10444
Vancouver
Guion-Almeida ML, Richieri-Costa A. Acrofrontofacionasal dysostosis: report of the third Brazilian family [Internet]. American Journal of Medical Genetics. 2003 ; 119A( 2): 238-241.[citado 2024 nov. 12 ] Available from: https://doi.org/10.1002/ajmg.a.10444
Artigo de periodico
Autosomal recessive acro-fronto-facio-nasal dysostosis associated with genitourinary anomalies (1989)
Richieri-Costa, Antonio; Montagnoli, Luiz Carlos; Kamiya, Tânia Yoshico
Source: American Journal of Medical Genetics. Unidade: HRAC
Subjects: DISOSTOSE CRÂNIOFACIAL, GENES RECESSIVOS, ANORMALIDADES UROGENITAIS
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ABNT
RICHIERI-COSTA, Antonio e MONTAGNOLI, Luiz Carlos e KAMIYA, Tânia Yoshico. Autosomal recessive acro-fronto-facio-nasal dysostosis associated with genitourinary anomalies. American Journal of Medical Genetics, v. 33, n. 1, p. 121-124, 1989Tradução . . Disponível em: https://doi.org/10.1002/ajmg.1320330118. Acesso em: 12 nov. 2024.
APA
Richieri-Costa, A., Montagnoli, L. C., & Kamiya, T. Y. (1989). Autosomal recessive acro-fronto-facio-nasal dysostosis associated with genitourinary anomalies. American Journal of Medical Genetics, 33( 1), 121-124. doi:10.1002/ajmg.1320330118
NLM
Richieri-Costa A, Montagnoli LC, Kamiya TY. Autosomal recessive acro-fronto-facio-nasal dysostosis associated with genitourinary anomalies [Internet]. American Journal of Medical Genetics. 1989 ; 33( 1): 121-124.[citado 2024 nov. 12 ] Available from: https://doi.org/10.1002/ajmg.1320330118
Vancouver
Richieri-Costa A, Montagnoli LC, Kamiya TY. Autosomal recessive acro-fronto-facio-nasal dysostosis associated with genitourinary anomalies [Internet]. American Journal of Medical Genetics. 1989 ; 33( 1): 121-124.[citado 2024 nov. 12 ] Available from: https://doi.org/10.1002/ajmg.1320330118
Artigo de periodico
Postaxial acrofacial dysostosis: report of a Brazilian patient (1989)
Richieri-Costa, Antonio; Guion-Almeida, Maria Leine
Source: American Journal of Medical Genetics. Unidade: HRAC
Subjects: GENÉTICA MÉDICA, DISOSTOSE CRÂNIOFACIAL
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
RICHIERI-COSTA, Antonio e GUION-ALMEIDA, Maria Leine. Postaxial acrofacial dysostosis: report of a Brazilian patient. American Journal of Medical Genetics, v. 33, n. 4, p. 447-449, 1989Tradução . . Disponível em: https://doi.org/10.1002/ajmg.1320330405. Acesso em: 12 nov. 2024.
APA
Richieri-Costa, A., & Guion-Almeida, M. L. (1989). Postaxial acrofacial dysostosis: report of a Brazilian patient. American Journal of Medical Genetics, 33( 4), 447-449. doi:10.1002/ajmg.1320330405
NLM
Richieri-Costa A, Guion-Almeida ML. Postaxial acrofacial dysostosis: report of a Brazilian patient [Internet]. American Journal of Medical Genetics. 1989 ; 33( 4): 447-449.[citado 2024 nov. 12 ] Available from: https://doi.org/10.1002/ajmg.1320330405
Vancouver
Richieri-Costa A, Guion-Almeida ML. Postaxial acrofacial dysostosis: report of a Brazilian patient [Internet]. American Journal of Medical Genetics. 1989 ; 33( 4): 447-449.[citado 2024 nov. 12 ] Available from: https://doi.org/10.1002/ajmg.1320330405
Artigo de periodico
A previously undescribed autosomal recessive multiple congenital anomalies/mental retardation (MCA/MR) syndrome with fronto-nasal dysostosis, cleft lip/palate, limb hypoplasia, and postaxial poly-syndactyly: acro-fronto-facio-nasal dysostosis syndrome (1985)
Richieri-Costa, Antonio; Colletto, G. M. D. D.; Gollop, T. R.; Masiero, D.
Source: American Journal of Medical Genetics. Unidade: HRAC
Subjects: ANORMALIDADES CONGÊNITAS, RETARDO MENTAL, FISSURA LÁBIOPALATINA, DISOSTOSE CRÂNIOFACIAL
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
RICHIERI-COSTA, Antonio et al. A previously undescribed autosomal recessive multiple congenital anomalies/mental retardation (MCA/MR) syndrome with fronto-nasal dysostosis, cleft lip/palate, limb hypoplasia, and postaxial poly-syndactyly: acro-fronto-facio-nasal dysostosis syndrome. American Journal of Medical Genetics, v. 20, n. 4, p. 631-638, 1985Tradução . . Disponível em: https://doi.org/10.1002/ajmg.1320200409. Acesso em: 12 nov. 2024.
APA
Richieri-Costa, A., Colletto, G. M. D. D., Gollop, T. R., & Masiero, D. (1985). A previously undescribed autosomal recessive multiple congenital anomalies/mental retardation (MCA/MR) syndrome with fronto-nasal dysostosis, cleft lip/palate, limb hypoplasia, and postaxial poly-syndactyly: acro-fronto-facio-nasal dysostosis syndrome. American Journal of Medical Genetics, 20( 4), 631-638. doi:10.1002/ajmg.1320200409
NLM
Richieri-Costa A, Colletto GMDD, Gollop TR, Masiero D. A previously undescribed autosomal recessive multiple congenital anomalies/mental retardation (MCA/MR) syndrome with fronto-nasal dysostosis, cleft lip/palate, limb hypoplasia, and postaxial poly-syndactyly: acro-fronto-facio-nasal dysostosis syndrome [Internet]. American Journal of Medical Genetics. 1985 ; 20( 4): 631-638.[citado 2024 nov. 12 ] Available from: https://doi.org/10.1002/ajmg.1320200409
Vancouver
Richieri-Costa A, Colletto GMDD, Gollop TR, Masiero D. A previously undescribed autosomal recessive multiple congenital anomalies/mental retardation (MCA/MR) syndrome with fronto-nasal dysostosis, cleft lip/palate, limb hypoplasia, and postaxial poly-syndactyly: acro-fronto-facio-nasal dysostosis syndrome [Internet]. American Journal of Medical Genetics. 1985 ; 20( 4): 631-638.[citado 2024 nov. 12 ] Available from: https://doi.org/10.1002/ajmg.1320200409
Artigo de periodico
Syndrome of acrofacial dysostosis, cleft lip/palate, and triphalangeal thumb in a Brazilian family [Brief clinical report] (1983)
Richieri-Costa, Antonio; Gollop, Thomaz Rafael; Colleto, G. M. D. D.
Source: American Journal of Medical Genetics. Unidade: HRAC
Subjects: DISOSTOSE CRÂNIOFACIAL, FISSURA LÁBIOPALATINA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
RICHIERI-COSTA, Antonio e GOLLOP, Thomaz Rafael e COLLETO, G. M. D. D. Syndrome of acrofacial dysostosis, cleft lip/palate, and triphalangeal thumb in a Brazilian family [Brief clinical report]. American Journal of Medical Genetics, v. 14, n. 2, p. 225-229, 1983Tradução . . Acesso em: 12 nov. 2024.
APA
Richieri-Costa, A., Gollop, T. R., & Colleto, G. M. D. D. (1983). Syndrome of acrofacial dysostosis, cleft lip/palate, and triphalangeal thumb in a Brazilian family [Brief clinical report]. American Journal of Medical Genetics, 14( 2), 225-229.
NLM
Richieri-Costa A, Gollop TR, Colleto GMDD. Syndrome of acrofacial dysostosis, cleft lip/palate, and triphalangeal thumb in a Brazilian family [Brief clinical report]. American Journal of Medical Genetics. 1983 ; 14( 2): 225-229.[citado 2024 nov. 12 ]
Vancouver
Richieri-Costa A, Gollop TR, Colleto GMDD. Syndrome of acrofacial dysostosis, cleft lip/palate, and triphalangeal thumb in a Brazilian family [Brief clinical report]. American Journal of Medical Genetics. 1983 ; 14( 2): 225-229.[citado 2024 nov. 12 ]

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