ReP USP - Resultado da busca

Artigo de periodico
Newly recognized autosomal recessive MCA/MR/overgrowth syndrome (1993)
Richieri-Costa, Antonio; Guion-Almeida, Maria Leine; Cohen Junior, M. Michael
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, Antonio e GUION-ALMEIDA, Maria Leine e COHEN JUNIOR, M. Michael. Newly recognized autosomal recessive MCA/MR/overgrowth syndrome. American Journal of Medical Genetics, v. 47, n. 2, p. 278-280, 1993Tradução . . Acesso em: 04 out. 2024.
APA
Richieri-Costa, A., Guion-Almeida, M. L., & Cohen Junior, M. M. (1993). Newly recognized autosomal recessive MCA/MR/overgrowth syndrome. American Journal of Medical Genetics, 47( 2), 278-280.
NLM
Richieri-Costa A, Guion-Almeida ML, Cohen Junior MM. Newly recognized autosomal recessive MCA/MR/overgrowth syndrome. American Journal of Medical Genetics. 1993 ; 47( 2): 278-280.[citado 2024 out. 04 ]
Vancouver
Richieri-Costa A, Guion-Almeida ML, Cohen Junior MM. Newly recognized autosomal recessive MCA/MR/overgrowth syndrome. American Journal of Medical Genetics. 1993 ; 47( 2): 278-280.[citado 2024 out. 04 ]
Artigo de periodico
Newly recognized blepharofacioskeletal syndrome (1993)
Richieri-Costa, Antonio; Guion-Almeida, Maria Leine; Rodini, Elaine Sbroggio de Oliveira; Pereira, S C D; Cohen Junior, M. Michael
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, Antonio et al. Newly recognized blepharofacioskeletal syndrome. American Journal of Medical Genetics, v. 46, n. 6, p. 620-622, 1993Tradução . . Disponível em: https://doi.org/10.1002/ajmg.1320460603. Acesso em: 04 out. 2024.
APA
Richieri-Costa, A., Guion-Almeida, M. L., Rodini, E. S. de O., Pereira, S. C. D., & Cohen Junior, M. M. (1993). Newly recognized blepharofacioskeletal syndrome. American Journal of Medical Genetics, 46( 6), 620-622. doi:10.1002/ajmg.1320460603
NLM
Richieri-Costa A, Guion-Almeida ML, Rodini ES de O, Pereira SCD, Cohen Junior MM. Newly recognized blepharofacioskeletal syndrome [Internet]. American Journal of Medical Genetics. 1993 ; 46( 6): 620-622.[citado 2024 out. 04 ] Available from: https://doi.org/10.1002/ajmg.1320460603
Vancouver
Richieri-Costa A, Guion-Almeida ML, Rodini ES de O, Pereira SCD, Cohen Junior MM. Newly recognized blepharofacioskeletal syndrome [Internet]. American Journal of Medical Genetics. 1993 ; 46( 6): 620-622.[citado 2024 out. 04 ] Available from: https://doi.org/10.1002/ajmg.1320460603
Artigo de periodico
Cleft palate-lateral synechiae syndrome: report on three new patients with additional findings and evidence for variability and heterogeneity (1993)
Nakata, Nancy Mizue Kokitsu; Guion-Almeida, Maria Leine; Richieri-Costa, Antonio
Source: American Journal of Medical Genetics. Unidade: HRAC
Subjects: ANORMALIDADES CRANIOFACIAIS, FISSURA PALATINA, RETARDO MENTAL
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
NAKATA, Nancy Mizue Kokitsu e GUION-ALMEIDA, Maria Leine e RICHIERI-COSTA, Antonio. Cleft palate-lateral synechiae syndrome: report on three new patients with additional findings and evidence for variability and heterogeneity. American Journal of Medical Genetics, v. 47, n. 1, p. 330-332, 1993Tradução . . Disponível em: https://doi.org/10.1002/ajmg.1320470307. Acesso em: 04 out. 2024.
APA
Nakata, N. M. K., Guion-Almeida, M. L., & Richieri-Costa, A. (1993). Cleft palate-lateral synechiae syndrome: report on three new patients with additional findings and evidence for variability and heterogeneity. American Journal of Medical Genetics, 47( 1), 330-332. doi:10.1002/ajmg.1320470307
NLM
Nakata NMK, Guion-Almeida ML, Richieri-Costa A. Cleft palate-lateral synechiae syndrome: report on three new patients with additional findings and evidence for variability and heterogeneity [Internet]. American Journal of Medical Genetics. 1993 ; 47( 1): 330-332.[citado 2024 out. 04 ] Available from: https://doi.org/10.1002/ajmg.1320470307
Vancouver
Nakata NMK, Guion-Almeida ML, Richieri-Costa A. Cleft palate-lateral synechiae syndrome: report on three new patients with additional findings and evidence for variability and heterogeneity [Internet]. American Journal of Medical Genetics. 1993 ; 47( 1): 330-332.[citado 2024 out. 04 ] Available from: https://doi.org/10.1002/ajmg.1320470307
Trabalho de evento-resumo periodico
Sindrome de bowen-amstrong: estudo clinico-genetico de dois pacientes (1993)
Rodini, E S O; Guion-Almeida, Maria Leine
Source: Revista Brasileira de Genetica = Brazilian Journal of Genetics. Conference titles: Congresso Nacional de Genetica. 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 GUION-ALMEIDA, Maria Leine. Sindrome de bowen-amstrong: estudo clinico-genetico de dois pacientes. Revista Brasileira de Genetica = Brazilian Journal of Genetics. [S.l.]: Hospital de Reabilitação de Anomalias Craniofaciais, Universidade de São Paulo. . Acesso em: 04 out. 2024. , 1993
APA
Rodini, E. S. O., & Guion-Almeida, M. L. (1993). Sindrome de bowen-amstrong: estudo clinico-genetico de dois pacientes. Revista Brasileira de Genetica = Brazilian Journal of Genetics. Hospital de Reabilitação de Anomalias Craniofaciais, Universidade de São Paulo.
NLM
Rodini ESO, Guion-Almeida ML. Sindrome de bowen-amstrong: estudo clinico-genetico de dois pacientes. Revista Brasileira de Genetica = Brazilian Journal of Genetics. 1993 ;16( 3 suppl.): 78.[citado 2024 out. 04 ]
Vancouver
Rodini ESO, Guion-Almeida ML. Sindrome de bowen-amstrong: estudo clinico-genetico de dois pacientes. Revista Brasileira de Genetica = Brazilian Journal of Genetics. 1993 ;16( 3 suppl.): 78.[citado 2024 out. 04 ]
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
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
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: 04 out. 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 out. 04 ]
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 out. 04 ]
Trabalho de evento-resumo periodico
Sindrome de dellemann: estudo clinico-genetico de um paciente (1993)
Guion-Almeida, Maria Leine; Nakata, N M K
Source: Revista Brasileira de Genetica = Brazilian Journal of Genetics. Conference titles: Congresso Nacional de Genetica. 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 NAKATA, N M K. Sindrome de dellemann: estudo clinico-genetico de um paciente. Revista Brasileira de Genetica = Brazilian Journal of Genetics. [S.l.]: Hospital de Reabilitação de Anomalias Craniofaciais, Universidade de São Paulo. . Acesso em: 04 out. 2024. , 1993
APA
Guion-Almeida, M. L., & Nakata, N. M. K. (1993). Sindrome de dellemann: estudo clinico-genetico de um paciente. Revista Brasileira de Genetica = Brazilian Journal of Genetics. Hospital de Reabilitação de Anomalias Craniofaciais, Universidade de São Paulo.
NLM
Guion-Almeida ML, Nakata NMK. Sindrome de dellemann: estudo clinico-genetico de um paciente. Revista Brasileira de Genetica = Brazilian Journal of Genetics. 1993 ;16( 3 suppl.): 79.[citado 2024 out. 04 ]
Vancouver
Guion-Almeida ML, Nakata NMK. Sindrome de dellemann: estudo clinico-genetico de um paciente. Revista Brasileira de Genetica = Brazilian Journal of Genetics. 1993 ;16( 3 suppl.): 79.[citado 2024 out. 04 ]
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
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, 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: 04 out. 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 out. 04 ]
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 out. 04 ]
Artigo de periodico
Conjoined twins: report of a Brazilian twin belonging to the category duplicatas incompleta, an atypical parasite twinning type (1993)
Richieri-Costa, Antonio; Guion-Almeida, Maria Leine; Frederigue Junior, Ulisses
Source: Birth Defects Original Article Series. Unidade: HRAC
Assunto: ANORMALIDADES MÚLTIPLAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
RICHIERI-COSTA, Antonio e GUION-ALMEIDA, Maria Leine e FREDERIGUE JUNIOR, Ulisses. Conjoined twins: report of a Brazilian twin belonging to the category duplicatas incompleta, an atypical parasite twinning type. Birth Defects Original Article Series, v. 29, n. 1, p. 273-277, 1993Tradução . . Acesso em: 04 out. 2024.
APA
Richieri-Costa, A., Guion-Almeida, M. L., & Frederigue Junior, U. (1993). Conjoined twins: report of a Brazilian twin belonging to the category duplicatas incompleta, an atypical parasite twinning type. Birth Defects Original Article Series, 29( 1), 273-277.
NLM
Richieri-Costa A, Guion-Almeida ML, Frederigue Junior U. Conjoined twins: report of a Brazilian twin belonging to the category duplicatas incompleta, an atypical parasite twinning type. Birth Defects Original Article Series. 1993 ; 29( 1): 273-277.[citado 2024 out. 04 ]
Vancouver
Richieri-Costa A, Guion-Almeida ML, Frederigue Junior U. Conjoined twins: report of a Brazilian twin belonging to the category duplicatas incompleta, an atypical parasite twinning type. Birth Defects Original Article Series. 1993 ; 29( 1): 273-277.[citado 2024 out. 04 ]
Artigo de periodico
Mandibulofacial dysostosis: report on two Brazilian families suggesting autosomal recessive inheritance (1993)
Richieri-Costa, Antonio; Bortolozo, M A; Lauris, José Roberto Pereira; Lauris, Rita de Cássia Moura Carvalho; Guion-Almeida, Maria Leine; Marques, D; Moreti, D
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, Antonio et al. Mandibulofacial dysostosis: report on two Brazilian families suggesting autosomal recessive inheritance. American Journal of Medical Genetics, v. 46, n. 6, p. 659-664, 1993Tradução . . Disponível em: https://doi.org/10.1002/ajmg.1320460611. Acesso em: 04 out. 2024.
APA
Richieri-Costa, A., Bortolozo, M. A., Lauris, J. R. P., Lauris, R. de C. M. C., Guion-Almeida, M. L., Marques, D., & Moreti, D. (1993). Mandibulofacial dysostosis: report on two Brazilian families suggesting autosomal recessive inheritance. American Journal of Medical Genetics, 46( 6), 659-664. doi:10.1002/ajmg.1320460611
NLM
Richieri-Costa A, Bortolozo MA, Lauris JRP, Lauris R de CMC, Guion-Almeida ML, Marques D, Moreti D. Mandibulofacial dysostosis: report on two Brazilian families suggesting autosomal recessive inheritance [Internet]. American Journal of Medical Genetics. 1993 ; 46( 6): 659-664.[citado 2024 out. 04 ] Available from: https://doi.org/10.1002/ajmg.1320460611
Vancouver
Richieri-Costa A, Bortolozo MA, Lauris JRP, Lauris R de CMC, Guion-Almeida ML, Marques D, Moreti D. Mandibulofacial dysostosis: report on two Brazilian families suggesting autosomal recessive inheritance [Internet]. American Journal of Medical Genetics. 1993 ; 46( 6): 659-664.[citado 2024 out. 04 ] Available from: https://doi.org/10.1002/ajmg.1320460611
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: 04 out. 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 out. 04 ] 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 out. 04 ] Available from: https://doi.org/10.1002/ajmg.1320470523

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