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Study of birth defects detected in a series of 2019 consecutive pediatric autopsies (2005)
Piram, Adriana; Peres, Luiz Cesar; Pina Neto, João Monteiro de
Source: Virchows Archiv. Conference titles: European Congress of Pathology. Unidade: FMRP
Subjects: AUTÓPSIA, DOENÇAS NEONATAIS E ANORMALIDADES
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
PIRAM, Adriana e PERES, Luiz Cesar e PINA NETO, João Monteiro de. Study of birth defects detected in a series of 2019 consecutive pediatric autopsies. Virchows Archiv. Heidelberg: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. . Acesso em: 07 out. 2024. , 2005
APA
Piram, A., Peres, L. C., & Pina Neto, J. M. de. (2005). Study of birth defects detected in a series of 2019 consecutive pediatric autopsies. Virchows Archiv. Heidelberg: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo.
NLM
Piram A, Peres LC, Pina Neto JM de. Study of birth defects detected in a series of 2019 consecutive pediatric autopsies. Virchows Archiv. 2005 ; 447( 2): 147.[citado 2024 out. 07 ]
Vancouver
Piram A, Peres LC, Pina Neto JM de. Study of birth defects detected in a series of 2019 consecutive pediatric autopsies. Virchows Archiv. 2005 ; 447( 2): 147.[citado 2024 out. 07 ]
Artigo de periodico
Newborn with malformations and a combined duplication of 9pter-q22 and 16q22-qter resulting from unbalanced segregation of a complex maternal translocation (2003)
Piram, Adriana; Ortolan, Daniela; Peres, Luiz César; Pina Neto, João Monteiro de; Riegel, Mariluce; Schinzel, Albert
Source: American Journal of Medical Genetics. Unidade: FMRP
Assunto: GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
PIRAM, Adriana et al. Newborn with malformations and a combined duplication of 9pter-q22 and 16q22-qter resulting from unbalanced segregation of a complex maternal translocation. American Journal of Medical Genetics, v. 120A, p. 247-252, 2003Tradução . . Disponível em: https://doi.org/10.1002/ajmg.a.10004. Acesso em: 07 out. 2024.
APA
Piram, A., Ortolan, D., Peres, L. C., Pina Neto, J. M. de, Riegel, M., & Schinzel, A. (2003). Newborn with malformations and a combined duplication of 9pter-q22 and 16q22-qter resulting from unbalanced segregation of a complex maternal translocation. American Journal of Medical Genetics, 120A, 247-252. doi:10.1002/ajmg.a.10004
NLM
Piram A, Ortolan D, Peres LC, Pina Neto JM de, Riegel M, Schinzel A. Newborn with malformations and a combined duplication of 9pter-q22 and 16q22-qter resulting from unbalanced segregation of a complex maternal translocation [Internet]. American Journal of Medical Genetics. 2003 ; 120A 247-252.[citado 2024 out. 07 ] Available from: https://doi.org/10.1002/ajmg.a.10004
Vancouver
Piram A, Ortolan D, Peres LC, Pina Neto JM de, Riegel M, Schinzel A. Newborn with malformations and a combined duplication of 9pter-q22 and 16q22-qter resulting from unbalanced segregation of a complex maternal translocation [Internet]. American Journal of Medical Genetics. 2003 ; 120A 247-252.[citado 2024 out. 07 ] Available from: https://doi.org/10.1002/ajmg.a.10004
Artigo de periodico
De novo unbalanded T(11Q;21Q) leading to a partial monosomy 21PTER-Q22.2 and 11Q24-QTER in a patient initially diagnosed as monosomy 21 (2001)
Riegel, M.; Baumer, A.; Piram, Adriana; Ortolan, Daniela; Peres, Luiz César; Pina Neto, João Monteiro de
Source: Genetic Counseling. Unidade: FMRP
Subjects: ACONSELHAMENTO GENÉTICO, CROMOSSOMOS HUMANOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
RIEGEL, M. et al. De novo unbalanded T(11Q;21Q) leading to a partial monosomy 21PTER-Q22.2 and 11Q24-QTER in a patient initially diagnosed as monosomy 21. Genetic Counseling, v. 12, n. 1, p. 69-75, 2001Tradução . . Acesso em: 07 out. 2024.
APA
Riegel, M., Baumer, A., Piram, A., Ortolan, D., Peres, L. C., & Pina Neto, J. M. de. (2001). De novo unbalanded T(11Q;21Q) leading to a partial monosomy 21PTER-Q22.2 and 11Q24-QTER in a patient initially diagnosed as monosomy 21. Genetic Counseling, 12( 1), 69-75.
NLM
Riegel M, Baumer A, Piram A, Ortolan D, Peres LC, Pina Neto JM de. De novo unbalanded T(11Q;21Q) leading to a partial monosomy 21PTER-Q22.2 and 11Q24-QTER in a patient initially diagnosed as monosomy 21. Genetic Counseling. 2001 ; 12( 1): 69-75.[citado 2024 out. 07 ]
Vancouver
Riegel M, Baumer A, Piram A, Ortolan D, Peres LC, Pina Neto JM de. De novo unbalanded T(11Q;21Q) leading to a partial monosomy 21PTER-Q22.2 and 11Q24-QTER in a patient initially diagnosed as monosomy 21. Genetic Counseling. 2001 ; 12( 1): 69-75.[citado 2024 out. 07 ]

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