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Agammaglobulinemia associated to chromosome 2 deletion (1996)
Wheba, J; Richieri-Costa, A; Costa-Carvalho, B T; Carneiro-Sampaio, M. M. S.; Sole, D; Naspitz, C K
Source: Archivos Argentinos de Alergia e Inmunologia Clinica. Conference titles: Simposio Internacional de Alergia e Inmunologia Clinica en Pediatria. Unidades: HRAC, ICB
Assunto: IMUNOLOGIA
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ABNT
WHEBA, J et al. Agammaglobulinemia associated to chromosome 2 deletion. Archivos Argentinos de Alergia e Inmunologia Clinica. [S.l.]: Hospital de Reabilitação de Anomalias Craniofaciais, Universidade de São Paulo. . Acesso em: 15 nov. 2024. , 1996
APA
Wheba, J., Richieri-Costa, A., Costa-Carvalho, B. T., Carneiro-Sampaio, M. M. S., Sole, D., & Naspitz, C. K. (1996). Agammaglobulinemia associated to chromosome 2 deletion. Archivos Argentinos de Alergia e Inmunologia Clinica. Hospital de Reabilitação de Anomalias Craniofaciais, Universidade de São Paulo.
NLM
Wheba J, Richieri-Costa A, Costa-Carvalho BT, Carneiro-Sampaio MMS, Sole D, Naspitz CK. Agammaglobulinemia associated to chromosome 2 deletion. Archivos Argentinos de Alergia e Inmunologia Clinica. 1996 ;27 19.[citado 2024 nov. 15 ]
Vancouver
Wheba J, Richieri-Costa A, Costa-Carvalho BT, Carneiro-Sampaio MMS, Sole D, Naspitz CK. Agammaglobulinemia associated to chromosome 2 deletion. Archivos Argentinos de Alergia e Inmunologia Clinica. 1996 ;27 19.[citado 2024 nov. 15 ]
Artigo de periodico
Hypertelorism: interobital growth, measurements, and pathogenetic considerations (1995)
Cohen Junior, M. Michael; Richieri-Costa, A; Guion-Almeida, Maria Leine; Saavedra, Dolores
Source: International Journal of Oral Maxillofacial Surgery. Unidade: HRAC
Assunto: GENÉTICA MÉDICA
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ABNT
COHEN JUNIOR, M. Michael et al. Hypertelorism: interobital growth, measurements, and pathogenetic considerations. International Journal of Oral Maxillofacial Surgery, v. 24, p. 387-395, 1995Tradução . . Disponível em: https://doi.org/10.1016/s0901-5027(05)80465-5. Acesso em: 15 nov. 2024.
APA
Cohen Junior, M. M., Richieri-Costa, A., Guion-Almeida, M. L., & Saavedra, D. (1995). Hypertelorism: interobital growth, measurements, and pathogenetic considerations. International Journal of Oral Maxillofacial Surgery, 24, 387-395. doi:10.1016/s0901-5027(05)80465-5
NLM
Cohen Junior MM, Richieri-Costa A, Guion-Almeida ML, Saavedra D. Hypertelorism: interobital growth, measurements, and pathogenetic considerations [Internet]. International Journal of Oral Maxillofacial Surgery. 1995 ;24 387-395.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1016/s0901-5027(05)80465-5
Vancouver
Cohen Junior MM, Richieri-Costa A, Guion-Almeida ML, Saavedra D. Hypertelorism: interobital growth, measurements, and pathogenetic considerations [Internet]. International Journal of Oral Maxillofacial Surgery. 1995 ;24 387-395.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1016/s0901-5027(05)80465-5
Artigo de periodico
Word-finding difficulties, verbal paraphasias, and verbal dyspraxia in ten individuals with fragile x syndrome (1995)
Spinelli, M; Rocha, A C O; Giacheti, C M; Richieri-Costa, A
Source: American Journal of Medical Genetics (Neuropsychiatric Genetics). Unidade: HRAC
Assunto: FONOAUDIOLOGIA
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ABNT
SPINELLI, M et al. Word-finding difficulties, verbal paraphasias, and verbal dyspraxia in ten individuals with fragile x syndrome. American Journal of Medical Genetics (Neuropsychiatric Genetics), v. 60, p. 39-43, 1995Tradução . . Disponível em: https://doi.org/10.1002/ajmg.1320600108. Acesso em: 15 nov. 2024.
APA
Spinelli, M., Rocha, A. C. O., Giacheti, C. M., & Richieri-Costa, A. (1995). Word-finding difficulties, verbal paraphasias, and verbal dyspraxia in ten individuals with fragile x syndrome. American Journal of Medical Genetics (Neuropsychiatric Genetics), 60, 39-43. doi:10.1002/ajmg.1320600108
NLM
Spinelli M, Rocha ACO, Giacheti CM, Richieri-Costa A. Word-finding difficulties, verbal paraphasias, and verbal dyspraxia in ten individuals with fragile x syndrome [Internet]. American Journal of Medical Genetics (Neuropsychiatric Genetics). 1995 ; 60 39-43.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1002/ajmg.1320600108
Vancouver
Spinelli M, Rocha ACO, Giacheti CM, Richieri-Costa A. Word-finding difficulties, verbal paraphasias, and verbal dyspraxia in ten individuals with fragile x syndrome [Internet]. American Journal of Medical Genetics (Neuropsychiatric Genetics). 1995 ; 60 39-43.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1002/ajmg.1320600108
Artigo de periodico
Newly recognized autosomal recessive faciothoracoskeletal syndrome (1994)
Richieri-Costa, A; Guion-Almeida, Maria Leine; Lauris, J R P; Ferreira, D M
Source: American Journal of Medical Genetics. Unidade: HRAC
Assunto: GENÉTICA
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ABNT
RICHIERI-COSTA, A et al. Newly recognized autosomal recessive faciothoracoskeletal syndrome. American Journal of Medical Genetics, v. 49, n. 2, p. 224-228, 1994Tradução . . Disponível em: https://doi.org/10.1002/ajmg.1320490213. Acesso em: 15 nov. 2024.
APA
Richieri-Costa, A., Guion-Almeida, M. L., Lauris, J. R. P., & Ferreira, D. M. (1994). Newly recognized autosomal recessive faciothoracoskeletal syndrome. American Journal of Medical Genetics, 49( 2), 224-228. doi:10.1002/ajmg.1320490213
NLM
Richieri-Costa A, Guion-Almeida ML, Lauris JRP, Ferreira DM. Newly recognized autosomal recessive faciothoracoskeletal syndrome [Internet]. American Journal of Medical Genetics. 1994 ; 49( 2): 224-228.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1002/ajmg.1320490213
Vancouver
Richieri-Costa A, Guion-Almeida ML, Lauris JRP, Ferreira DM. Newly recognized autosomal recessive faciothoracoskeletal syndrome [Internet]. American Journal of Medical Genetics. 1994 ; 49( 2): 224-228.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1002/ajmg.1320490213
Artigo de periodico
Heteropagus epignathus: report on a Brazilian twin (1993)
Richieri-Costa, A; Guion-Almeida, Maria Leine
Source: Birth Defects: Original Article Series. Unidade: HRAC
Assunto: ODONTOLOGIA
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ABNT
RICHIERI-COSTA, A e GUION-ALMEIDA, Maria Leine. Heteropagus epignathus: report on a Brazilian twin. Birth Defects: Original Article Series, v. 29, n. 1, p. 383-387, 1993Tradução . . Acesso em: 15 nov. 2024.
APA
Richieri-Costa, A., & Guion-Almeida, M. L. (1993). Heteropagus epignathus: report on a Brazilian twin. Birth Defects: Original Article Series, 29( 1), 383-387.
NLM
Richieri-Costa A, Guion-Almeida ML. Heteropagus epignathus: report on a Brazilian twin. Birth Defects: Original Article Series. 1993 ; 29( 1): 383-387.[citado 2024 nov. 15 ]
Vancouver
Richieri-Costa A, Guion-Almeida ML. Heteropagus epignathus: report on a Brazilian twin. Birth Defects: Original Article Series. 1993 ; 29( 1): 383-387.[citado 2024 nov. 15 ]
Artigo de periodico
Holoprosencephaly, harmatomatous growth of the cerebrum, dysplatic gangliocytoma of the cerebellum, unique brain anomalies, and renal agenesis in a Brazilian infant born to a diabetic mother: a clinical and pathologic study (1993)
Richieri-Costa, A; Frederique Junior, U; Guion-Almeida, Maria Leine
Source: Birth Defects: Original Article Series. Unidade: HRAC
Assunto: ODONTOLOGIA
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ABNT
RICHIERI-COSTA, A e FREDERIQUE JUNIOR, U e GUION-ALMEIDA, Maria Leine. Holoprosencephaly, harmatomatous growth of the cerebrum, dysplatic gangliocytoma of the cerebellum, unique brain anomalies, and renal agenesis in a Brazilian infant born to a diabetic mother: a clinical and pathologic study. Birth Defects: Original Article Series, v. 29, n. 1, p. 389-394, 1993Tradução . . Acesso em: 15 nov. 2024.
APA
Richieri-Costa, A., Frederique Junior, U., & Guion-Almeida, M. L. (1993). Holoprosencephaly, harmatomatous growth of the cerebrum, dysplatic gangliocytoma of the cerebellum, unique brain anomalies, and renal agenesis in a Brazilian infant born to a diabetic mother: a clinical and pathologic study. Birth Defects: Original Article Series, 29( 1), 389-394.
NLM
Richieri-Costa A, Frederique Junior U, Guion-Almeida ML. Holoprosencephaly, harmatomatous growth of the cerebrum, dysplatic gangliocytoma of the cerebellum, unique brain anomalies, and renal agenesis in a Brazilian infant born to a diabetic mother: a clinical and pathologic study. Birth Defects: Original Article Series. 1993 ; 29( 1): 389-394.[citado 2024 nov. 15 ]
Vancouver
Richieri-Costa A, Frederique Junior U, Guion-Almeida ML. Holoprosencephaly, harmatomatous growth of the cerebrum, dysplatic gangliocytoma of the cerebellum, unique brain anomalies, and renal agenesis in a Brazilian infant born to a diabetic mother: a clinical and pathologic study. Birth Defects: Original Article Series. 1993 ; 29( 1): 389-394.[citado 2024 nov. 15 ]
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
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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: 15 nov. 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 nov. 15 ] 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 nov. 15 ] 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
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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: 15 nov. 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 nov. 15 ] 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 nov. 15 ] 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
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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: 15 nov. 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 nov. 15 ]
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 nov. 15 ]
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
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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: 15 nov. 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 nov. 15 ] 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 nov. 15 ] 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
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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: 15 nov. 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 nov. 15 ] 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 nov. 15 ] 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
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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: 15 nov. 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 nov. 15 ]
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 nov. 15 ]
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: 15 nov. 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 nov. 15 ] 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 nov. 15 ] 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
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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: 15 nov. 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 nov. 15 ] 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 nov. 15 ] Available from: https://doi.org/10.1002/ajmg.1320440616
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: 15 nov. 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 nov. 15 ]
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 nov. 15 ]
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: 15 nov. 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 nov. 15 ]
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 nov. 15 ]
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: 15 nov. 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 nov. 15 ]
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 nov. 15 ]
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: 15 nov. 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 nov. 15 ] 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 nov. 15 ] Available from: https://doi.org/10.1002/ajmg.1320430606
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: 15 nov. 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 nov. 15 ] 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 nov. 15 ] 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: 15 nov. 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 nov. 15 ]
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 nov. 15 ]

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