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Artigo de periodico
Microphthalmia, linear skin defects, callosal agenesis, and cleft palate in a patient with deletion at Xp22.3p22.2 (2020)
Pittoli, Siulan Vendramini Paulovich ; Souza, Rosana Maria Candido ; Quiezi, Rodrigo Gonçalves; Zechi-Ceide, Roseli Maria ; Nakata, Nancy Mizue Kokitsu ; Jehee, Fernanda Sarquis; Ribeiro-Bicudo, Lucilene Arilho ; FitzPatrick, David R. ; Guion-Almeida, Maria Leine; Richieri-Costa, Antonio
Fonte: Journal of Pediatric Genetics. Unidades: HRAC, HRACF
Assuntos: AGENESIA, FISSURA PALATINA, DELEÇÃO DE GENES
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
PITTOLI, Siulan Vendramini Paulovich et al. Microphthalmia, linear skin defects, callosal agenesis, and cleft palate in a patient with deletion at Xp22.3p22.2. Journal of Pediatric Genetics, v. 9, n. 4, p. 258-262, 2020Tradução . . Disponível em: https://doi.org/10.1055/s-0039-3402047. Acesso em: 18 out. 2024.
APA
Pittoli, S. V. P., Souza, R. M. C., Quiezi, R. G., Zechi-Ceide, R. M., Nakata, N. M. K., Jehee, F. S., et al. (2020). Microphthalmia, linear skin defects, callosal agenesis, and cleft palate in a patient with deletion at Xp22.3p22.2. Journal of Pediatric Genetics, 9( 4), 258-262. doi:10.1055/s-0039-3402047
NLM
Pittoli SVP, Souza RMC, Quiezi RG, Zechi-Ceide RM, Nakata NMK, Jehee FS, Ribeiro-Bicudo LA, FitzPatrick DR, Guion-Almeida ML, Richieri-Costa A. Microphthalmia, linear skin defects, callosal agenesis, and cleft palate in a patient with deletion at Xp22.3p22.2 [Internet]. Journal of Pediatric Genetics. 2020 ; 9( 4): 258-262.[citado 2024 out. 18 ] Available from: https://doi.org/10.1055/s-0039-3402047
Vancouver
Pittoli SVP, Souza RMC, Quiezi RG, Zechi-Ceide RM, Nakata NMK, Jehee FS, Ribeiro-Bicudo LA, FitzPatrick DR, Guion-Almeida ML, Richieri-Costa A. Microphthalmia, linear skin defects, callosal agenesis, and cleft palate in a patient with deletion at Xp22.3p22.2 [Internet]. Journal of Pediatric Genetics. 2020 ; 9( 4): 258-262.[citado 2024 out. 18 ] Available from: https://doi.org/10.1055/s-0039-3402047
Artigo de periodico
Multisystem involvement in a patient with a PTCH1 mutation: clinical and imaging findings (2017)
Richieri-Costa, Antonio; Pittoli, Siulan Vendramini Paulovich; Nakata, Nancy Mizue Kokitsu; Ceide, Roseli Maria Zechi; Alvarez, Camila Wenceslau; Bicudo, Lucilene Arilho Ribeiro
Fonte: Journal of Pediatric Genetics. Unidade: HRAC
Assuntos: HOLOPROSENCEFALIA, MUTAÇÃO GENÉTICA, FENÓTIPOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
RICHIERI-COSTA, Antonio et al. Multisystem involvement in a patient with a PTCH1 mutation: clinical and imaging findings. Journal of Pediatric Genetics, v. 6, n. 2, p. 103-106, 2017Tradução . . Disponível em: https://doi.org/10.1055/s-0036-1588028. Acesso em: 18 out. 2024.
APA
Richieri-Costa, A., Pittoli, S. V. P., Nakata, N. M. K., Ceide, R. M. Z., Alvarez, C. W., & Bicudo, L. A. R. (2017). Multisystem involvement in a patient with a PTCH1 mutation: clinical and imaging findings. Journal of Pediatric Genetics, 6( 2), 103-106. doi:10.1055/s-0036-1588028
NLM
Richieri-Costa A, Pittoli SVP, Nakata NMK, Ceide RMZ, Alvarez CW, Bicudo LAR. Multisystem involvement in a patient with a PTCH1 mutation: clinical and imaging findings [Internet]. Journal of Pediatric Genetics. 2017 ; 6( 2): 103-106.[citado 2024 out. 18 ] Available from: https://doi.org/10.1055/s-0036-1588028
Vancouver
Richieri-Costa A, Pittoli SVP, Nakata NMK, Ceide RMZ, Alvarez CW, Bicudo LAR. Multisystem involvement in a patient with a PTCH1 mutation: clinical and imaging findings [Internet]. Journal of Pediatric Genetics. 2017 ; 6( 2): 103-106.[citado 2024 out. 18 ] Available from: https://doi.org/10.1055/s-0036-1588028
Artigo de periodico
Chromothripsis with at least 12 breaks at 1p36.33-p35.3 in a boy with multiple congenital anomalies (2015)
Gamba, Bruno Faulin; Richieri-Costa, Antonio ; Costa, Silvia; Rosenberg, Carla ; Ribeiro-Bicudo, Lucilene Arilho
Fonte: Molecular Genetics and Genomics. Unidades: HRAC, IB
Assuntos: DOENÇAS GENÉTICAS, CROMOSSOMOS HUMANOS (ANOMALIAS), MALFORMAÇÕES
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
GAMBA, Bruno Faulin et al. Chromothripsis with at least 12 breaks at 1p36.33-p35.3 in a boy with multiple congenital anomalies. Molecular Genetics and Genomics, n. Ju 2015, p. on-line, 2015Tradução . . Disponível em: https://doi.org/10.1007/s00438-015-1072-0. Acesso em: 18 out. 2024.
APA
Gamba, B. F., Richieri-Costa, A., Costa, S., Rosenberg, C., & Ribeiro-Bicudo, L. A. (2015). Chromothripsis with at least 12 breaks at 1p36.33-p35.3 in a boy with multiple congenital anomalies. Molecular Genetics and Genomics, ( Ju 2015), on-line. doi:10.1007/s00438-015-1072-0
NLM
Gamba BF, Richieri-Costa A, Costa S, Rosenberg C, Ribeiro-Bicudo LA. Chromothripsis with at least 12 breaks at 1p36.33-p35.3 in a boy with multiple congenital anomalies [Internet]. Molecular Genetics and Genomics. 2015 ;( Ju 2015): on-line.[citado 2024 out. 18 ] Available from: https://doi.org/10.1007/s00438-015-1072-0
Vancouver
Gamba BF, Richieri-Costa A, Costa S, Rosenberg C, Ribeiro-Bicudo LA. Chromothripsis with at least 12 breaks at 1p36.33-p35.3 in a boy with multiple congenital anomalies [Internet]. Molecular Genetics and Genomics. 2015 ;( Ju 2015): on-line.[citado 2024 out. 18 ] Available from: https://doi.org/10.1007/s00438-015-1072-0
Artigo de periodico
Odontogenic keratocyst and multiple supernumerary teeth in a patient with Ehlers-Danlos syndrome: a case report and review of the literature (2008)
Ferreira Júnior, Osny; Cardoso, Camila Lopes; Capelozza, Ana Lúcia Álvares; Yaedú, Renato Yassutaba Faria; Richieri-Costa, Antonio
Fonte: Quintessence International. Unidade: FOB
Assuntos: DENTE SUPRANUMERÁRIO, CISTO PRIMORDIAL, ODONTOGÊNESE, TECIDO CONJUNTIVO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
FERREIRA JÚNIOR, Osny et al. Odontogenic keratocyst and multiple supernumerary teeth in a patient with Ehlers-Danlos syndrome: a case report and review of the literature. Quintessence International, v. 39, n. 3, p. 251-256, 2008Tradução . . Acesso em: 18 out. 2024.
APA
Ferreira Júnior, O., Cardoso, C. L., Capelozza, A. L. Á., Yaedú, R. Y. F., & Richieri-Costa, A. (2008). Odontogenic keratocyst and multiple supernumerary teeth in a patient with Ehlers-Danlos syndrome: a case report and review of the literature. Quintessence International, 39( 3), 251-256.
NLM
Ferreira Júnior O, Cardoso CL, Capelozza ALÁ, Yaedú RYF, Richieri-Costa A. Odontogenic keratocyst and multiple supernumerary teeth in a patient with Ehlers-Danlos syndrome: a case report and review of the literature. Quintessence International. 2008 ; 39( 3): 251-256.[citado 2024 out. 18 ]
Vancouver
Ferreira Júnior O, Cardoso CL, Capelozza ALÁ, Yaedú RYF, Richieri-Costa A. Odontogenic keratocyst and multiple supernumerary teeth in a patient with Ehlers-Danlos syndrome: a case report and review of the literature. Quintessence International. 2008 ; 39( 3): 251-256.[citado 2024 out. 18 ]
Artigo de periodico
Frontonasal dysplasia: analysis of 21 cases and literature review (1996)
Guion-Almeida, Maria Leine; Richieri-Costa, Antonio; Saavedra, Dolores; Cohen Junior, M. Michael
Fonte: International Journal of Maxillofacial Surgery. Unidade: HRAC
Assuntos: SÍNDROMES OROFACIODIGITAIS, FISSURA LÁBIOPALATINA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
GUION-ALMEIDA, Maria Leine et al. Frontonasal dysplasia: analysis of 21 cases and literature review. International Journal of Maxillofacial Surgery, v. 25, n. 2, p. 91-97, 1996Tradução . . Disponível em: https://doi.org/10.1016/s0901-5027(96)80048-8. Acesso em: 18 out. 2024.
APA
Guion-Almeida, M. L., Richieri-Costa, A., Saavedra, D., & Cohen Junior, M. M. (1996). Frontonasal dysplasia: analysis of 21 cases and literature review. International Journal of Maxillofacial Surgery, 25( 2), 91-97. doi:10.1016/s0901-5027(96)80048-8
NLM
Guion-Almeida ML, Richieri-Costa A, Saavedra D, Cohen Junior MM. Frontonasal dysplasia: analysis of 21 cases and literature review [Internet]. International Journal of Maxillofacial Surgery. 1996 ; 25( 2): 91-97.[citado 2024 out. 18 ] Available from: https://doi.org/10.1016/s0901-5027(96)80048-8
Vancouver
Guion-Almeida ML, Richieri-Costa A, Saavedra D, Cohen Junior MM. Frontonasal dysplasia: analysis of 21 cases and literature review [Internet]. International Journal of Maxillofacial Surgery. 1996 ; 25( 2): 91-97.[citado 2024 out. 18 ] Available from: https://doi.org/10.1016/s0901-5027(96)80048-8
Artigo de periodico
Partial monosomy 13 and 21 due to a familial 13/21 translocation (1978)
Otto, Priscila Guimarães; Toledo, Sérgio; Richieri-Costa, Antonio; Otto, Paulo A ; Vianna-Morgante, Angela M ; Kasahara, Sanae
Fonte: Human Genetics. Unidade: IB
Assunto: ANORMALIDADES CROMOSSÔMICAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
OTTO, Priscila Guimarães et al. Partial monosomy 13 and 21 due to a familial 13/21 translocation. Human Genetics, v. 41, p. 243-250, 1978Tradução . . Disponível em: https://doi.org/10.1007/bf00284757. Acesso em: 18 out. 2024.
APA
Otto, P. G., Toledo, S., Richieri-Costa, A., Otto, P. A., Vianna-Morgante, A. M., & Kasahara, S. (1978). Partial monosomy 13 and 21 due to a familial 13/21 translocation. Human Genetics, 41, 243-250. doi:10.1007/bf00284757
NLM
Otto PG, Toledo S, Richieri-Costa A, Otto PA, Vianna-Morgante AM, Kasahara S. Partial monosomy 13 and 21 due to a familial 13/21 translocation [Internet]. Human Genetics. 1978 ; 41 243-250.[citado 2024 out. 18 ] Available from: https://doi.org/10.1007/bf00284757
Vancouver
Otto PG, Toledo S, Richieri-Costa A, Otto PA, Vianna-Morgante AM, Kasahara S. Partial monosomy 13 and 21 due to a familial 13/21 translocation [Internet]. Human Genetics. 1978 ; 41 243-250.[citado 2024 out. 18 ] Available from: https://doi.org/10.1007/bf00284757

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