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Artigo de periodico
Mental retardation, structural anomalies of the central nervous system, anophthalmia and abnormal nares: a new MCA/MR syndrome of unknown cause (1993)
Richieri-Costa, A; Guion-Almeida, Maria Leine
Source: American Journal of Medical Genetics. Unidade: HRAC
Assunto: GENÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
RICHIERI-COSTA, A e GUION-ALMEIDA, Maria Leine. Mental retardation, structural anomalies of the central nervous system, anophthalmia and abnormal nares: a new MCA/MR syndrome of unknown cause. American Journal of Medical Genetics, v. 47, n. 5, p. 702-706, 1993Tradução . . Disponível em: https://doi.org/10.1002/ajmg.1320470523. Acesso em: 01 jun. 2024.
APA
Richieri-Costa, A., & Guion-Almeida, M. L. (1993). Mental retardation, structural anomalies of the central nervous system, anophthalmia and abnormal nares: a new MCA/MR syndrome of unknown cause. American Journal of Medical Genetics, 47( 5), 702-706. doi:10.1002/ajmg.1320470523
NLM
Richieri-Costa A, Guion-Almeida ML. Mental retardation, structural anomalies of the central nervous system, anophthalmia and abnormal nares: a new MCA/MR syndrome of unknown cause [Internet]. American Journal of Medical Genetics. 1993 ; 47( 5): 702-706.[citado 2024 jun. 01 ] Available from: https://doi.org/10.1002/ajmg.1320470523
Vancouver
Richieri-Costa A, Guion-Almeida ML. Mental retardation, structural anomalies of the central nervous system, anophthalmia and abnormal nares: a new MCA/MR syndrome of unknown cause [Internet]. American Journal of Medical Genetics. 1993 ; 47( 5): 702-706.[citado 2024 jun. 01 ] Available from: https://doi.org/10.1002/ajmg.1320470523
Artigo de periodico
Autosomal recessive short stature, Robin sequence, cleft mandible, pre/postaxial hand anomalies, and clubfeet in male patients (1993)
Richieri-Costa, A; Pereira, Sonia Cristina Silveira
Source: American Journal of Medical Genetics. Unidade: HRAC
Assunto: GENÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
RICHIERI-COSTA, A e PEREIRA, Sonia Cristina Silveira. Autosomal recessive short stature, Robin sequence, cleft mandible, pre/postaxial hand anomalies, and clubfeet in male patients. American Journal of Medical Genetics, v. 47, n. 5, p. 707-709, 1993Tradução . . Disponível em: https://doi.org/10.1002/ajmg.1320470524. Acesso em: 01 jun. 2024.
APA
Richieri-Costa, A., & Pereira, S. C. S. (1993). Autosomal recessive short stature, Robin sequence, cleft mandible, pre/postaxial hand anomalies, and clubfeet in male patients. American Journal of Medical Genetics, 47( 5), 707-709. doi:10.1002/ajmg.1320470524
NLM
Richieri-Costa A, Pereira SCS. Autosomal recessive short stature, Robin sequence, cleft mandible, pre/postaxial hand anomalies, and clubfeet in male patients [Internet]. American Journal of Medical Genetics. 1993 ; 47( 5): 707-709.[citado 2024 jun. 01 ] Available from: https://doi.org/10.1002/ajmg.1320470524
Vancouver
Richieri-Costa A, Pereira SCS. Autosomal recessive short stature, Robin sequence, cleft mandible, pre/postaxial hand anomalies, and clubfeet in male patients [Internet]. American Journal of Medical Genetics. 1993 ; 47( 5): 707-709.[citado 2024 jun. 01 ] Available from: https://doi.org/10.1002/ajmg.1320470524
Artigo de periodico
Ectodermal dysplasia, ectrodactyly, clefting, anophthalmia/microphthalmia, and genitourinary anomalies: nosology of goltz-gorlin syndrome versus EEC syndrome (1992)
Rodini, E S O; Nardi, A; Guion-Almeida, Maria Leine; Richieri-Costa, A
Source: American Journal of Medical Genetics. Unidade: HRAC
Assunto: GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
RODINI, E S O et al. Ectodermal dysplasia, ectrodactyly, clefting, anophthalmia/microphthalmia, and genitourinary anomalies: nosology of goltz-gorlin syndrome versus EEC syndrome. American Journal of Medical Genetics, v. 42, n. 3, p. 276-280, 1992Tradução . . Acesso em: 01 jun. 2024.
APA
Rodini, E. S. O., Nardi, A., Guion-Almeida, M. L., & Richieri-Costa, A. (1992). Ectodermal dysplasia, ectrodactyly, clefting, anophthalmia/microphthalmia, and genitourinary anomalies: nosology of goltz-gorlin syndrome versus EEC syndrome. American Journal of Medical Genetics, 42( 3), 276-280.
NLM
Rodini ESO, Nardi A, Guion-Almeida ML, Richieri-Costa A. Ectodermal dysplasia, ectrodactyly, clefting, anophthalmia/microphthalmia, and genitourinary anomalies: nosology of goltz-gorlin syndrome versus EEC syndrome. American Journal of Medical Genetics. 1992 ; 42( 3): 276-280.[citado 2024 jun. 01 ]
Vancouver
Rodini ESO, Nardi A, Guion-Almeida ML, Richieri-Costa A. Ectodermal dysplasia, ectrodactyly, clefting, anophthalmia/microphthalmia, and genitourinary anomalies: nosology of goltz-gorlin syndrome versus EEC syndrome. American Journal of Medical Genetics. 1992 ; 42( 3): 276-280.[citado 2024 jun. 01 ]
Artigo de periodico
Marden-walker-like syndrome without psychomotor retardation: report of a Brazilian girl born to consaguineous parents (1992)
Ende, J J van den; Bever, Y V; Rodini, E S O; Richieri-Costa, A
Source: American Journal of Medical Genetics. Unidade: HRAC
Assunto: MEDICINA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ENDE, J J van den et al. Marden-walker-like syndrome without psychomotor retardation: report of a Brazilian girl born to consaguineous parents. American Journal of Medical Genetics, v. 42, n. 4, p. 467-469, 1992Tradução . . Disponível em: https://doi.org/10.1002/ajmg.1320420411. Acesso em: 01 jun. 2024.
APA
Ende, J. J. van den, Bever, Y. V., Rodini, E. S. O., & Richieri-Costa, A. (1992). Marden-walker-like syndrome without psychomotor retardation: report of a Brazilian girl born to consaguineous parents. American Journal of Medical Genetics, 42( 4), 467-469. doi:10.1002/ajmg.1320420411
NLM
Ende JJ van den, Bever YV, Rodini ESO, Richieri-Costa A. Marden-walker-like syndrome without psychomotor retardation: report of a Brazilian girl born to consaguineous parents [Internet]. American Journal of Medical Genetics. 1992 ; 42( 4): 467-469.[citado 2024 jun. 01 ] Available from: https://doi.org/10.1002/ajmg.1320420411
Vancouver
Ende JJ van den, Bever YV, Rodini ESO, Richieri-Costa A. Marden-walker-like syndrome without psychomotor retardation: report of a Brazilian girl born to consaguineous parents [Internet]. American Journal of Medical Genetics. 1992 ; 42( 4): 467-469.[citado 2024 jun. 01 ] Available from: https://doi.org/10.1002/ajmg.1320420411
Artigo de periodico
Trigonocephaly (1992)
Zanini, S A; Paglioli Neto, E; Viterbo, F; Richieri-Costa, A; Tershakowec, M
Source: Journal of Craniofacial Surgery. Unidade: HRAC
Assunto: GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ZANINI, S A et al. Trigonocephaly. Journal of Craniofacial Surgery, v. 3 , n. 2 , p. se 1992, 1992Tradução . . Disponível em: https://doi.org/10.1097/00006534-198508000-00005. Acesso em: 01 jun. 2024.
APA
Zanini, S. A., Paglioli Neto, E., Viterbo, F., Richieri-Costa, A., & Tershakowec, M. (1992). Trigonocephaly. Journal of Craniofacial Surgery, 3 ( 2 ), se 1992. doi:10.1097/00006534-198508000-00005
NLM
Zanini SA, Paglioli Neto E, Viterbo F, Richieri-Costa A, Tershakowec M. Trigonocephaly [Internet]. Journal of Craniofacial Surgery. 1992 ;3 ( 2 ): se 1992.[citado 2024 jun. 01 ] Available from: https://doi.org/10.1097/00006534-198508000-00005
Vancouver
Zanini SA, Paglioli Neto E, Viterbo F, Richieri-Costa A, Tershakowec M. Trigonocephaly [Internet]. Journal of Craniofacial Surgery. 1992 ;3 ( 2 ): se 1992.[citado 2024 jun. 01 ] Available from: https://doi.org/10.1097/00006534-198508000-00005
Artigo de periodico
Hypoglossia-hypodactyly syndrome in a Brazilian child: clinical and surgical aspects (1992)
Zanini, S A; Seara, Simone; Willhelm, Ricardo; Heitz, Claiton; Tershakowec, Mark; Richieri-Costa, A
Source: Journal of Craniofacial Surgery. Unidade: HRAC
Assunto: GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ZANINI, S A et al. Hypoglossia-hypodactyly syndrome in a Brazilian child: clinical and surgical aspects. Journal of Craniofacial Surgery, v. 3, n. 1, p. 33-34, 1992Tradução . . Acesso em: 01 jun. 2024.
APA
Zanini, S. A., Seara, S., Willhelm, R., Heitz, C., Tershakowec, M., & Richieri-Costa, A. (1992). Hypoglossia-hypodactyly syndrome in a Brazilian child: clinical and surgical aspects. Journal of Craniofacial Surgery, 3( 1), 33-34.
NLM
Zanini SA, Seara S, Willhelm R, Heitz C, Tershakowec M, Richieri-Costa A. Hypoglossia-hypodactyly syndrome in a Brazilian child: clinical and surgical aspects. Journal of Craniofacial Surgery. 1992 ; 3( 1): 33-34.[citado 2024 jun. 01 ]
Vancouver
Zanini SA, Seara S, Willhelm R, Heitz C, Tershakowec M, Richieri-Costa A. Hypoglossia-hypodactyly syndrome in a Brazilian child: clinical and surgical aspects. Journal of Craniofacial Surgery. 1992 ; 3( 1): 33-34.[citado 2024 jun. 01 ]
Artigo de periodico
Autosomal recessive blepharoptosis, cleft lip/palate, dental anomalies, and ectrodactyly (1992)
Rodini, E S O; Richieri-Costa, A
Source: American Journal of Medical Genetics. Unidade: HRAC
Assunto: GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
RODINI, E S O e RICHIERI-COSTA, A. Autosomal recessive blepharoptosis, cleft lip/palate, dental anomalies, and ectrodactyly. American Journal of Medical Genetics, v. 42, n. 3 , p. 340-342, 1992Tradução . . Disponível em: https://doi.org/10.1002/ajmg.1320420317. Acesso em: 01 jun. 2024.
APA
Rodini, E. S. O., & Richieri-Costa, A. (1992). Autosomal recessive blepharoptosis, cleft lip/palate, dental anomalies, and ectrodactyly. American Journal of Medical Genetics, 42( 3 ), 340-342. doi:10.1002/ajmg.1320420317
NLM
Rodini ESO, Richieri-Costa A. Autosomal recessive blepharoptosis, cleft lip/palate, dental anomalies, and ectrodactyly [Internet]. American Journal of Medical Genetics. 1992 ; 42( 3 ): 340-342.[citado 2024 jun. 01 ] Available from: https://doi.org/10.1002/ajmg.1320420317
Vancouver
Rodini ESO, Richieri-Costa A. Autosomal recessive blepharoptosis, cleft lip/palate, dental anomalies, and ectrodactyly [Internet]. American Journal of Medical Genetics. 1992 ; 42( 3 ): 340-342.[citado 2024 jun. 01 ] Available from: https://doi.org/10.1002/ajmg.1320420317
Artigo de periodico
Acro-fronto-facio-nasal dysostosis: report of a new Brazilian family (1992)
Richieri-Costa, A; Guion-Almeida, Maria Leine; Pagnan, Nina Amalia Brancia
Source: American Journal of Medical Genetics. Unidade: HRAC
Assunto: GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
RICHIERI-COSTA, A e GUION-ALMEIDA, Maria Leine e PAGNAN, Nina Amalia Brancia. Acro-fronto-facio-nasal dysostosis: report of a new Brazilian family. American Journal of Medical Genetics, v. 44, n. 6, p. 800-802, 1992Tradução . . Disponível em: https://doi.org/10.1002/ajmg.1320440616. Acesso em: 01 jun. 2024.
APA
Richieri-Costa, A., Guion-Almeida, M. L., & Pagnan, N. A. B. (1992). Acro-fronto-facio-nasal dysostosis: report of a new Brazilian family. American Journal of Medical Genetics, 44( 6), 800-802. doi:10.1002/ajmg.1320440616
NLM
Richieri-Costa A, Guion-Almeida ML, Pagnan NAB. Acro-fronto-facio-nasal dysostosis: report of a new Brazilian family [Internet]. American Journal of Medical Genetics. 1992 ; 44( 6): 800-802.[citado 2024 jun. 01 ] Available from: https://doi.org/10.1002/ajmg.1320440616
Vancouver
Richieri-Costa A, Guion-Almeida ML, Pagnan NAB. Acro-fronto-facio-nasal dysostosis: report of a new Brazilian family [Internet]. American Journal of Medical Genetics. 1992 ; 44( 6): 800-802.[citado 2024 jun. 01 ] Available from: https://doi.org/10.1002/ajmg.1320440616
Artigo de periodico
Short stature, mental retardation, eye anomalies, and cleft lip/palate (1992)
Richieri-Costa, A; Guion-Almeida, Maria Leine
Source: American Journal of Medical Genetics. Unidade: HRAC
Assunto: ODONTOLOGIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
RICHIERI-COSTA, A e GUION-ALMEIDA, Maria Leine. Short stature, mental retardation, eye anomalies, and cleft lip/palate. American Journal of Medical Genetics, v. 42, n. 4, p. 449-452, 1992Tradução . . Disponível em: https://doi.org/10.1002/ajmg.1320420407. Acesso em: 01 jun. 2024.
APA
Richieri-Costa, A., & Guion-Almeida, M. L. (1992). Short stature, mental retardation, eye anomalies, and cleft lip/palate. American Journal of Medical Genetics, 42( 4), 449-452. doi:10.1002/ajmg.1320420407
NLM
Richieri-Costa A, Guion-Almeida ML. Short stature, mental retardation, eye anomalies, and cleft lip/palate [Internet]. American Journal of Medical Genetics. 1992 ; 42( 4): 449-452.[citado 2024 jun. 01 ] Available from: https://doi.org/10.1002/ajmg.1320420407
Vancouver
Richieri-Costa A, Guion-Almeida ML. Short stature, mental retardation, eye anomalies, and cleft lip/palate [Internet]. American Journal of Medical Genetics. 1992 ; 42( 4): 449-452.[citado 2024 jun. 01 ] Available from: https://doi.org/10.1002/ajmg.1320420407
Artigo de periodico
Brief clinical report. Autosomal recessive cleft lip / palate , ectodermal dysplasia , and minor anomalies: report of a brazilian family (1992)
Richieri-Costa, A; Guion-Almeida, Maria Leine; Freire Maia, N; Pinheiro, M
Source: American Journal of a Brazilian Family. Unidade: HRAC
Assunto: ODONTOLOGIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
RICHIERI-COSTA, A et al. Brief clinical report. Autosomal recessive cleft lip / palate , ectodermal dysplasia , and minor anomalies: report of a brazilian family. American Journal of a Brazilian Family, v. 44, n. 2 , p. se 1992, 1992Tradução . . Acesso em: 01 jun. 2024.
APA
Richieri-Costa, A., Guion-Almeida, M. L., Freire Maia, N., & Pinheiro, M. (1992). Brief clinical report. Autosomal recessive cleft lip / palate , ectodermal dysplasia , and minor anomalies: report of a brazilian family. American Journal of a Brazilian Family, 44( 2 ), se 1992.
NLM
Richieri-Costa A, Guion-Almeida ML, Freire Maia N, Pinheiro M. Brief clinical report. Autosomal recessive cleft lip / palate , ectodermal dysplasia , and minor anomalies: report of a brazilian family. American Journal of a Brazilian Family. 1992 ;44( 2 ): se 1992.[citado 2024 jun. 01 ]
Vancouver
Richieri-Costa A, Guion-Almeida ML, Freire Maia N, Pinheiro M. Brief clinical report. Autosomal recessive cleft lip / palate , ectodermal dysplasia , and minor anomalies: report of a brazilian family. American Journal of a Brazilian Family. 1992 ;44( 2 ): se 1992.[citado 2024 jun. 01 ]
Artigo de periodico
Mental retardation, microbrachycephaly, hypotelorism, palpebral ptosis, thin/long face, cleft lip, and lumbosacral/pelvic anomalies (1992)
Richieri-Costa, A; Guion-Almeida, Maria Leine; Ramos, A L
Source: American Journal of Medical Genetics. Unidade: HRAC
Assunto: GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
RICHIERI-COSTA, A e GUION-ALMEIDA, Maria Leine e RAMOS, A L. Mental retardation, microbrachycephaly, hypotelorism, palpebral ptosis, thin/long face, cleft lip, and lumbosacral/pelvic anomalies. American Journal of Medical Genetics, v. 43, n. 3, p. 565-568, 1992Tradução . . Acesso em: 01 jun. 2024.
APA
Richieri-Costa, A., Guion-Almeida, M. L., & Ramos, A. L. (1992). Mental retardation, microbrachycephaly, hypotelorism, palpebral ptosis, thin/long face, cleft lip, and lumbosacral/pelvic anomalies. American Journal of Medical Genetics, 43( 3), 565-568.
NLM
Richieri-Costa A, Guion-Almeida ML, Ramos AL. Mental retardation, microbrachycephaly, hypotelorism, palpebral ptosis, thin/long face, cleft lip, and lumbosacral/pelvic anomalies. American Journal of Medical Genetics. 1992 ; 43( 3): 565-568.[citado 2024 jun. 01 ]
Vancouver
Richieri-Costa A, Guion-Almeida ML, Ramos AL. Mental retardation, microbrachycephaly, hypotelorism, palpebral ptosis, thin/long face, cleft lip, and lumbosacral/pelvic anomalies. American Journal of Medical Genetics. 1992 ; 43( 3): 565-568.[citado 2024 jun. 01 ]
Trabalho de evento-resumo
Avaliacao de pacientes com a sindrome de goldenhar em relacao a abordagem terapeutica fonoaudiologica (1992)
Caldana, M L; Mandra, P P; Richieri-Costa, A; Bever, Y V; Eude, Y V B
Source: Anais. Conference titles: Semana Comemorativa do Aniversario da Faculdade de Odontologia de Bauru. Unidade: HRAC
Assunto: FONOAUDIOLOGIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
CALDANA, M L et al. Avaliacao de pacientes com a sindrome de goldenhar em relacao a abordagem terapeutica fonoaudiologica. 1992, Anais.. Bauru: Fob-Usp, 1992. . Acesso em: 01 jun. 2024.
APA
Caldana, M. L., Mandra, P. P., Richieri-Costa, A., Bever, Y. V., & Eude, Y. V. B. (1992). Avaliacao de pacientes com a sindrome de goldenhar em relacao a abordagem terapeutica fonoaudiologica. In Anais. Bauru: Fob-Usp.
NLM
Caldana ML, Mandra PP, Richieri-Costa A, Bever YV, Eude YVB. Avaliacao de pacientes com a sindrome de goldenhar em relacao a abordagem terapeutica fonoaudiologica. Anais. 1992 ;[citado 2024 jun. 01 ]
Vancouver
Caldana ML, Mandra PP, Richieri-Costa A, Bever YV, Eude YVB. Avaliacao de pacientes com a sindrome de goldenhar em relacao a abordagem terapeutica fonoaudiologica. Anais. 1992 ;[citado 2024 jun. 01 ]
Artigo de periodico
CNS midline anomalies in the Opitz G/BBB syndrome: report on 12 Brazilian patients (1992)
Guion-Almeida, Maria Leine; Richieri-Costa, A
Source: American Journal of Medical Genetics. Unidade: HRAC
Assunto: GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
GUION-ALMEIDA, Maria Leine e RICHIERI-COSTA, A. CNS midline anomalies in the Opitz G/BBB syndrome: report on 12 Brazilian patients. American Journal of Medical Genetics, v. 43, n. 6, p. 918-928, 1992Tradução . . Acesso em: 01 jun. 2024.
APA
Guion-Almeida, M. L., & Richieri-Costa, A. (1992). CNS midline anomalies in the Opitz G/BBB syndrome: report on 12 Brazilian patients. American Journal of Medical Genetics, 43( 6), 918-928.
NLM
Guion-Almeida ML, Richieri-Costa A. CNS midline anomalies in the Opitz G/BBB syndrome: report on 12 Brazilian patients. American Journal of Medical Genetics. 1992 ; 43( 6): 918-928.[citado 2024 jun. 01 ]
Vancouver
Guion-Almeida ML, Richieri-Costa A. CNS midline anomalies in the Opitz G/BBB syndrome: report on 12 Brazilian patients. American Journal of Medical Genetics. 1992 ; 43( 6): 918-928.[citado 2024 jun. 01 ]
Artigo de periodico
Acrocallosal syndrome: report of a Brazilian girl (1992)
Guion-Almeida, Maria Leine; Richieri-Costa, A
Source: American Journal of Medical Genetics. Unidade: HRAC
Assunto: GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
GUION-ALMEIDA, Maria Leine e RICHIERI-COSTA, A. Acrocallosal syndrome: report of a Brazilian girl. American Journal of Medical Genetics, v. 43, n. 6, p. 938-941, 1992Tradução . . Disponível em: https://doi.org/10.1002/ajmg.1320430606. Acesso em: 01 jun. 2024.
APA
Guion-Almeida, M. L., & Richieri-Costa, A. (1992). Acrocallosal syndrome: report of a Brazilian girl. American Journal of Medical Genetics, 43( 6), 938-941. doi:10.1002/ajmg.1320430606
NLM
Guion-Almeida ML, Richieri-Costa A. Acrocallosal syndrome: report of a Brazilian girl [Internet]. American Journal of Medical Genetics. 1992 ; 43( 6): 938-941.[citado 2024 jun. 01 ] Available from: https://doi.org/10.1002/ajmg.1320430606
Vancouver
Guion-Almeida ML, Richieri-Costa A. Acrocallosal syndrome: report of a Brazilian girl [Internet]. American Journal of Medical Genetics. 1992 ; 43( 6): 938-941.[citado 2024 jun. 01 ] Available from: https://doi.org/10.1002/ajmg.1320430606
Artigo de periodico
Postaxial acrofacial dysostosis: report on two patients (1992)
Pereira, S C S; Rocha, C M G; Guion-Almeida, Maria Leine; Richieri-Costa, A
Source: American Journal of Medical Genetics. Unidade: HRAC
Assunto: GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
PEREIRA, S C S et al. Postaxial acrofacial dysostosis: report on two patients. American Journal of Medical Genetics, v. 44, n. 3, p. 274-279, 1992Tradução . . Disponível em: https://doi.org/10.1002/ajmg.1320440303. Acesso em: 01 jun. 2024.
APA
Pereira, S. C. S., Rocha, C. M. G., Guion-Almeida, M. L., & Richieri-Costa, A. (1992). Postaxial acrofacial dysostosis: report on two patients. American Journal of Medical Genetics, 44( 3), 274-279. doi:10.1002/ajmg.1320440303
NLM
Pereira SCS, Rocha CMG, Guion-Almeida ML, Richieri-Costa A. Postaxial acrofacial dysostosis: report on two patients [Internet]. American Journal of Medical Genetics. 1992 ; 44( 3): 274-279.[citado 2024 jun. 01 ] Available from: https://doi.org/10.1002/ajmg.1320440303
Vancouver
Pereira SCS, Rocha CMG, Guion-Almeida ML, Richieri-Costa A. Postaxial acrofacial dysostosis: report on two patients [Internet]. American Journal of Medical Genetics. 1992 ; 44( 3): 274-279.[citado 2024 jun. 01 ] Available from: https://doi.org/10.1002/ajmg.1320440303
Artigo de periodico
Short stature, Robin sequence, cleft mandible pre/postaxial hand anomalies, and clubfoot: a new autosomal recessive syndrome (1992)
Richieri-Costa, A; Pereira, S C S
Source: American Journal of Medical Genetics. Unidade: HRAC
Subjects: GENÉTICA MÉDICA, MEDICINA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
RICHIERI-COSTA, A e PEREIRA, S C S. Short stature, Robin sequence, cleft mandible pre/postaxial hand anomalies, and clubfoot: a new autosomal recessive syndrome. American Journal of Medical Genetics, v. 42, n. 5, p. 681-687, 1992Tradução . . Disponível em: https://doi.org/10.1002/ajmg.1320420511. Acesso em: 01 jun. 2024.
APA
Richieri-Costa, A., & Pereira, S. C. S. (1992). Short stature, Robin sequence, cleft mandible pre/postaxial hand anomalies, and clubfoot: a new autosomal recessive syndrome. American Journal of Medical Genetics, 42( 5), 681-687. doi:10.1002/ajmg.1320420511
NLM
Richieri-Costa A, Pereira SCS. Short stature, Robin sequence, cleft mandible pre/postaxial hand anomalies, and clubfoot: a new autosomal recessive syndrome [Internet]. American Journal of Medical Genetics. 1992 ; 42( 5): 681-687.[citado 2024 jun. 01 ] Available from: https://doi.org/10.1002/ajmg.1320420511
Vancouver
Richieri-Costa A, Pereira SCS. Short stature, Robin sequence, cleft mandible pre/postaxial hand anomalies, and clubfoot: a new autosomal recessive syndrome [Internet]. American Journal of Medical Genetics. 1992 ; 42( 5): 681-687.[citado 2024 jun. 01 ] Available from: https://doi.org/10.1002/ajmg.1320420511
Artigo de periodico
Callosal agenesis, iris coloboma and megacolon in a Brazilian boy with Rubinstein-Taybi syndrome (1992)
Guion-Almeida, Maria Leine; Richieri-Costa, A
Source: American Journal of Medical Genetics. Unidade: HRAC
Assunto: GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
GUION-ALMEIDA, Maria Leine e RICHIERI-COSTA, A. Callosal agenesis, iris coloboma and megacolon in a Brazilian boy with Rubinstein-Taybi syndrome. American Journal of Medical Genetics, v. 43, n. 6, p. 929-931, 1992Tradução . . Acesso em: 01 jun. 2024.
APA
Guion-Almeida, M. L., & Richieri-Costa, A. (1992). Callosal agenesis, iris coloboma and megacolon in a Brazilian boy with Rubinstein-Taybi syndrome. American Journal of Medical Genetics, 43( 6), 929-931.
NLM
Guion-Almeida ML, Richieri-Costa A. Callosal agenesis, iris coloboma and megacolon in a Brazilian boy with Rubinstein-Taybi syndrome. American Journal of Medical Genetics. 1992 ; 43( 6): 929-931.[citado 2024 jun. 01 ]
Vancouver
Guion-Almeida ML, Richieri-Costa A. Callosal agenesis, iris coloboma and megacolon in a Brazilian boy with Rubinstein-Taybi syndrome. American Journal of Medical Genetics. 1992 ; 43( 6): 929-931.[citado 2024 jun. 01 ]
Artigo de periodico
Autosomal recessive cleft lip palate ectodermal dysplasia, and minor acral anomalies: report of a Brazilian family (1992)
Richieri-Costa, A; Guion-Almeida, Maria Leine; Freire-Maia, N; Pinheiro, M
Source: American Journal of Medical Genetics. Unidade: HRAC
Assunto: GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
RICHIERI-COSTA, A et al. Autosomal recessive cleft lip palate ectodermal dysplasia, and minor acral anomalies: report of a Brazilian family. American Journal of Medical Genetics, v. 44, n. 2, p. 158-162, 1992Tradução . . Disponível em: https://doi.org/10.1002/ajmg.1320440208. Acesso em: 01 jun. 2024.
APA
Richieri-Costa, A., Guion-Almeida, M. L., Freire-Maia, N., & Pinheiro, M. (1992). Autosomal recessive cleft lip palate ectodermal dysplasia, and minor acral anomalies: report of a Brazilian family. American Journal of Medical Genetics, 44( 2), 158-162. doi:10.1002/ajmg.1320440208
NLM
Richieri-Costa A, Guion-Almeida ML, Freire-Maia N, Pinheiro M. Autosomal recessive cleft lip palate ectodermal dysplasia, and minor acral anomalies: report of a Brazilian family [Internet]. American Journal of Medical Genetics. 1992 ; 44( 2): 158-162.[citado 2024 jun. 01 ] Available from: https://doi.org/10.1002/ajmg.1320440208
Vancouver
Richieri-Costa A, Guion-Almeida ML, Freire-Maia N, Pinheiro M. Autosomal recessive cleft lip palate ectodermal dysplasia, and minor acral anomalies: report of a Brazilian family [Internet]. American Journal of Medical Genetics. 1992 ; 44( 2): 158-162.[citado 2024 jun. 01 ] Available from: https://doi.org/10.1002/ajmg.1320440208
Artigo de periodico
Aarskog syndrome in a Brazilian boy born to consanguineous parents (1992)
Guion-Almeida, Maria Leine; Richieri-Costa, A
Source: American Journal of Medical Genetics. Unidade: HRAC
Assunto: GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
GUION-ALMEIDA, Maria Leine e RICHIERI-COSTA, A. Aarskog syndrome in a Brazilian boy born to consanguineous parents. American Journal of Medical Genetics, v. 43, n. 5, p. 808-810, 1992Tradução . . Disponível em: https://doi.org/10.1002/ajmg.1320430511. Acesso em: 01 jun. 2024.
APA
Guion-Almeida, M. L., & Richieri-Costa, A. (1992). Aarskog syndrome in a Brazilian boy born to consanguineous parents. American Journal of Medical Genetics, 43( 5), 808-810. doi:10.1002/ajmg.1320430511
NLM
Guion-Almeida ML, Richieri-Costa A. Aarskog syndrome in a Brazilian boy born to consanguineous parents [Internet]. American Journal of Medical Genetics. 1992 ; 43( 5): 808-810.[citado 2024 jun. 01 ] Available from: https://doi.org/10.1002/ajmg.1320430511
Vancouver
Guion-Almeida ML, Richieri-Costa A. Aarskog syndrome in a Brazilian boy born to consanguineous parents [Internet]. American Journal of Medical Genetics. 1992 ; 43( 5): 808-810.[citado 2024 jun. 01 ] Available from: https://doi.org/10.1002/ajmg.1320430511
Trabalho de evento-resumo
Holoprosencephaly , harmatomatous growth of the cerebrum dysplasic gangliocytoma of cerebellum, unique brain anomalies, and renal agenesis in a brazilian infant born to a diabetic mother: a clinical and pathological study (1991)
Richieri-Costa, A; Frederique Junior, U; Guion-Almeida, Maria Leine
Source: Abstracts. Conference titles: International Workshop on Fetal Genetic Pathology. Unidade: HRAC
Assunto: GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
RICHIERI-COSTA, A e FREDERIQUE JUNIOR, U e GUION-ALMEIDA, Maria Leine. Holoprosencephaly , harmatomatous growth of the cerebrum dysplasic gangliocytoma of cerebellum, unique brain anomalies, and renal agenesis in a brazilian infant born to a diabetic mother: a clinical and pathological study. 1991, Anais.. Montana: Shodair Children S Hospital, 1991. . Acesso em: 01 jun. 2024.
APA
Richieri-Costa, A., Frederique Junior, U., & Guion-Almeida, M. L. (1991). Holoprosencephaly , harmatomatous growth of the cerebrum dysplasic gangliocytoma of cerebellum, unique brain anomalies, and renal agenesis in a brazilian infant born to a diabetic mother: a clinical and pathological study. In Abstracts. Montana: Shodair Children S Hospital.
NLM
Richieri-Costa A, Frederique Junior U, Guion-Almeida ML. Holoprosencephaly , harmatomatous growth of the cerebrum dysplasic gangliocytoma of cerebellum, unique brain anomalies, and renal agenesis in a brazilian infant born to a diabetic mother: a clinical and pathological study. Abstracts. 1991 ;[citado 2024 jun. 01 ]
Vancouver
Richieri-Costa A, Frederique Junior U, Guion-Almeida ML. Holoprosencephaly , harmatomatous growth of the cerebrum dysplasic gangliocytoma of cerebellum, unique brain anomalies, and renal agenesis in a brazilian infant born to a diabetic mother: a clinical and pathological study. Abstracts. 1991 ;[citado 2024 jun. 01 ]

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