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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: 08 maio 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 maio 08 ] 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 maio 08 ] 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: 08 maio 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 maio 08 ] 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 maio 08 ] 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: 08 maio 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 maio 08 ]
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 maio 08 ]
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: 08 maio 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 maio 08 ] 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 maio 08 ] 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: 08 maio 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 maio 08 ] 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 maio 08 ] 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: 08 maio 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 maio 08 ]
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 maio 08 ]
Artigo de periodico
Sporadic, idiopathic mca syndrome with mandibulofacial dysostosis and tibial hemimelia (1991)
Richieri-Costa, A; Guion-Almeida, Maria Leine
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. Sporadic, idiopathic mca syndrome with mandibulofacial dysostosis and tibial hemimelia. American Journal of Medical Genetics, v. 41, n. 3 , p. 330-2, 1991Tradução . . Disponível em: https://doi.org/10.1002/ajmg.1320410314. Acesso em: 08 maio 2024.
APA
Richieri-Costa, A., & Guion-Almeida, M. L. (1991). Sporadic, idiopathic mca syndrome with mandibulofacial dysostosis and tibial hemimelia. American Journal of Medical Genetics, 41( 3 ), 330-2. doi:10.1002/ajmg.1320410314
NLM
Richieri-Costa A, Guion-Almeida ML. Sporadic, idiopathic mca syndrome with mandibulofacial dysostosis and tibial hemimelia [Internet]. American Journal of Medical Genetics. 1991 ;41( 3 ): 330-2.[citado 2024 maio 08 ] Available from: https://doi.org/10.1002/ajmg.1320410314
Vancouver
Richieri-Costa A, Guion-Almeida ML. Sporadic, idiopathic mca syndrome with mandibulofacial dysostosis and tibial hemimelia [Internet]. American Journal of Medical Genetics. 1991 ;41( 3 ): 330-2.[citado 2024 maio 08 ] Available from: https://doi.org/10.1002/ajmg.1320410314
Trabalho de evento-resumo
Conjoined twins: report of brazilian twin pair belonging to the category duplicitas incompleta ( atypical parasite twin ) (1991)
Richieri-Costa, A; Guion-Almeida, Maria Leine; Frederique Junior, U
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 GUION-ALMEIDA, Maria Leine e FREDERIQUE JUNIOR, U. Conjoined twins: report of brazilian twin pair belonging to the category duplicitas incompleta ( atypical parasite twin ). 1991, Anais.. Montana: Shodair Children S Hospital, 1991. . Acesso em: 08 maio 2024.
APA
Richieri-Costa, A., Guion-Almeida, M. L., & Frederique Junior, U. (1991). Conjoined twins: report of brazilian twin pair belonging to the category duplicitas incompleta ( atypical parasite twin ). In Abstracts. Montana: Shodair Children S Hospital.
NLM
Richieri-Costa A, Guion-Almeida ML, Frederique Junior U. Conjoined twins: report of brazilian twin pair belonging to the category duplicitas incompleta ( atypical parasite twin ). Abstracts. 1991 ;[citado 2024 maio 08 ]
Vancouver
Richieri-Costa A, Guion-Almeida ML, Frederique Junior U. Conjoined twins: report of brazilian twin pair belonging to the category duplicitas incompleta ( atypical parasite twin ). Abstracts. 1991 ;[citado 2024 maio 08 ]
Artigo de periodico
Antecubital pterygium and cleft lip/palate presenting as signs of the nail-patella syndrome: report of a Brazilian family (1991)
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
RICHIERI-COSTA, A. Antecubital pterygium and cleft lip/palate presenting as signs of the nail-patella syndrome: report of a Brazilian family. American Journal of Medical Genetics, v. 38, n. Ja 1991, p. 9-12, 1991Tradução . . Disponível em: https://doi.org/10.1002/ajmg.1320380103. Acesso em: 08 maio 2024.
APA
Richieri-Costa, A. (1991). Antecubital pterygium and cleft lip/palate presenting as signs of the nail-patella syndrome: report of a Brazilian family. American Journal of Medical Genetics, 38( Ja 1991), 9-12. doi:10.1002/ajmg.1320380103
NLM
Richieri-Costa A. Antecubital pterygium and cleft lip/palate presenting as signs of the nail-patella syndrome: report of a Brazilian family [Internet]. American Journal of Medical Genetics. 1991 ; 38( Ja 1991): 9-12.[citado 2024 maio 08 ] Available from: https://doi.org/10.1002/ajmg.1320380103
Vancouver
Richieri-Costa A. Antecubital pterygium and cleft lip/palate presenting as signs of the nail-patella syndrome: report of a Brazilian family [Internet]. American Journal of Medical Genetics. 1991 ; 38( Ja 1991): 9-12.[citado 2024 maio 08 ] Available from: https://doi.org/10.1002/ajmg.1320380103
Artigo de periodico
Autosomal dominant tibial hemimelia-polysyndactyly-triphalangeal thumbs syndrome: report of a Brazilian family (1990)
Richieri-Costa, A; Miranda, E; Kamiya, T Y; Freire-Maia, D V
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 dominant tibial hemimelia-polysyndactyly-triphalangeal thumbs syndrome: report of a Brazilian family. American Journal of Medical Genetics, v. 36, n. 1 , p. 1-6, 1990Tradução . . Disponível em: https://doi.org/10.1002/ajmg.1320360102. Acesso em: 08 maio 2024.
APA
Richieri-Costa, A., Miranda, E., Kamiya, T. Y., & Freire-Maia, D. V. (1990). Autosomal dominant tibial hemimelia-polysyndactyly-triphalangeal thumbs syndrome: report of a Brazilian family. American Journal of Medical Genetics, 36( 1 ), 1-6. doi:10.1002/ajmg.1320360102
NLM
Richieri-Costa A, Miranda E, Kamiya TY, Freire-Maia DV. Autosomal dominant tibial hemimelia-polysyndactyly-triphalangeal thumbs syndrome: report of a Brazilian family [Internet]. American Journal of Medical Genetics. 1990 ; 36( 1 ): 1-6.[citado 2024 maio 08 ] Available from: https://doi.org/10.1002/ajmg.1320360102
Vancouver
Richieri-Costa A, Miranda E, Kamiya TY, Freire-Maia DV. Autosomal dominant tibial hemimelia-polysyndactyly-triphalangeal thumbs syndrome: report of a Brazilian family [Internet]. American Journal of Medical Genetics. 1990 ; 36( 1 ): 1-6.[citado 2024 maio 08 ] Available from: https://doi.org/10.1002/ajmg.1320360102
Artigo de periodico
Rapp-hodgkin syndrome: report of a Brazilian family (1990)
Rodini, E O S; Freitas, J A S; Richieri-Costa, A
Source: American Journal of Medical Genetics. Unidades: HRAC, FOB
Assunto: GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
RODINI, E O S e FREITAS, J A S e RICHIERI-COSTA, A. Rapp-hodgkin syndrome: report of a Brazilian family. American Journal of Medical Genetics, v. 36, n. 4 , p. 463-466, 1990Tradução . . Acesso em: 08 maio 2024.
APA
Rodini, E. O. S., Freitas, J. A. S., & Richieri-Costa, A. (1990). Rapp-hodgkin syndrome: report of a Brazilian family. American Journal of Medical Genetics, 36( 4 ), 463-466.
NLM
Rodini EOS, Freitas JAS, Richieri-Costa A. Rapp-hodgkin syndrome: report of a Brazilian family. American Journal of Medical Genetics. 1990 ; 36( 4 ): 463-466.[citado 2024 maio 08 ]
Vancouver
Rodini EOS, Freitas JAS, Richieri-Costa A. Rapp-hodgkin syndrome: report of a Brazilian family. American Journal of Medical Genetics. 1990 ; 36( 4 ): 463-466.[citado 2024 maio 08 ]
Artigo de periodico
EEC syndrome: report on 20 new patients, clinical and genetic considerations (1990)
Rodini, E O S; 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 O S e RICHIERI-COSTA, A. EEC syndrome: report on 20 new patients, clinical and genetic considerations. American Journal of Medical Genetics, v. 37, n. 1, p. 42-53, 1990Tradução . . Disponível em: https://doi.org/10.1002/ajmg.1320370112. Acesso em: 08 maio 2024.
APA
Rodini, E. O. S., & Richieri-Costa, A. (1990). EEC syndrome: report on 20 new patients, clinical and genetic considerations. American Journal of Medical Genetics, 37( 1), 42-53. doi:10.1002/ajmg.1320370112
NLM
Rodini EOS, Richieri-Costa A. EEC syndrome: report on 20 new patients, clinical and genetic considerations [Internet]. American Journal of Medical Genetics. 1990 ; 37( 1): 42-53.[citado 2024 maio 08 ] Available from: https://doi.org/10.1002/ajmg.1320370112
Vancouver
Rodini EOS, Richieri-Costa A. EEC syndrome: report on 20 new patients, clinical and genetic considerations [Internet]. American Journal of Medical Genetics. 1990 ; 37( 1): 42-53.[citado 2024 maio 08 ] Available from: https://doi.org/10.1002/ajmg.1320370112

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