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Artigo de periodico
Altered regulation of DPF3, a member of the SWI/SNF complexes, underlies the 14q24 renal cancer susceptibility locus (2021)
Colli, Leandro Machado ; Jessop, Lea; Myers, Timothy A; Camp, Sabrina Y; Machiela, Mitchell J; Choi, Jiyeon; Cunha, Renato Luiz Guerino ; Onabajo, Olusegun; Mills, Grace C; Schmid, Virginia; Brodie, Seth A.; Delattre, Olivier; Mole, David R; Purdue, Mark P; Yu, Kai; Brown, Kevin M; Chanock, Stephen J.
Fonte: The American Journal of Human Genetics. Unidade: FMRP
Assuntos: NEOPLASIAS RENAIS, IMUNOTERAPIA
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ABNT
COLLI, Leandro Machado et al. Altered regulation of DPF3, a member of the SWI/SNF complexes, underlies the 14q24 renal cancer susceptibility locus. The American Journal of Human Genetics, v. 108, n. 9, p. 1590-1610, 2021Tradução . . Disponível em: https://doi.org/10.1016/j.ajhg.2021.07.009. Acesso em: 27 out. 2025.
APA
Colli, L. M., Jessop, L., Myers, T. A., Camp, S. Y., Machiela, M. J., Choi, J., et al. (2021). Altered regulation of DPF3, a member of the SWI/SNF complexes, underlies the 14q24 renal cancer susceptibility locus. The American Journal of Human Genetics, 108( 9), 1590-1610. doi:10.1016/j.ajhg.2021.07.009
NLM
Colli LM, Jessop L, Myers TA, Camp SY, Machiela MJ, Choi J, Cunha RLG, Onabajo O, Mills GC, Schmid V, Brodie SA, Delattre O, Mole DR, Purdue MP, Yu K, Brown KM, Chanock SJ. Altered regulation of DPF3, a member of the SWI/SNF complexes, underlies the 14q24 renal cancer susceptibility locus [Internet]. The American Journal of Human Genetics. 2021 ; 108( 9): 1590-1610.[citado 2025 out. 27 ] Available from: https://doi.org/10.1016/j.ajhg.2021.07.009
Vancouver
Colli LM, Jessop L, Myers TA, Camp SY, Machiela MJ, Choi J, Cunha RLG, Onabajo O, Mills GC, Schmid V, Brodie SA, Delattre O, Mole DR, Purdue MP, Yu K, Brown KM, Chanock SJ. Altered regulation of DPF3, a member of the SWI/SNF complexes, underlies the 14q24 renal cancer susceptibility locus [Internet]. The American Journal of Human Genetics. 2021 ; 108( 9): 1590-1610.[citado 2025 out. 27 ] Available from: https://doi.org/10.1016/j.ajhg.2021.07.009
Artigo de periodico
Haploinsufficiency of a spliceosomal GTPase encoded by EFTUD2 causes mandibulofacial dysostosis with microcephaly (2012)
Lines, Matthew A.; Huang, Lijia; Schwartzentruber, Jeremy; Douglas, Stuart L.; Lynch, Danielle C.; Beaulieu, Chandree; Guion-Almeida, Maria Leine; Zechi-Ceide, Roseli Maria ; Gener, Blanca; Gillessen-Kaesbach, Gabriele; Nava, Caroline; Baujat, Geneviève; Horn, Denise; Kini, Usha; Caliebe, Almuth; Alanay, Yasemin; Utine, Gulen Eda; Lev, Dorit; Kohlhase, Jürgen; Grix, Arthur W.; Lohmann, Dietmar R.; Hehr, Ute; Böhm, Detlef; FORGE Canada Consortium; Majewski, Jacek; Bulman, Dennis E.; Wieczorek, Dagmar; Boycott, Kym M.
Fonte: The American Journal of Human Genetics. Unidade: HRAC
Assuntos: DISOSTOSE MANDIBULOFACIAL, ANORMALIDADES CRANIOFACIAIS, TRANSTORNOS GLOBAIS DO DESENVOLVIMENTO INFANTIL
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LINES, Matthew A. et al. Haploinsufficiency of a spliceosomal GTPase encoded by EFTUD2 causes mandibulofacial dysostosis with microcephaly. The American Journal of Human Genetics, v. 90, n. 2, p. 369-377, 2012Tradução . . Disponível em: http://ac.els-cdn.com/S0002929712000407/1-s2.0-S0002929712000407-main.pdf?_tid=9e02e0be-273c-11e2-8ec4-00000aab0f26&acdnat=1352115387_9b121eaf2f4d65b8ce34daed5d6fd017. Acesso em: 27 out. 2025.
APA
Lines, M. A., Huang, L., Schwartzentruber, J., Douglas, S. L., Lynch, D. C., Beaulieu, C., et al. (2012). Haploinsufficiency of a spliceosomal GTPase encoded by EFTUD2 causes mandibulofacial dysostosis with microcephaly. The American Journal of Human Genetics, 90( 2), 369-377. Recuperado de http://ac.els-cdn.com/S0002929712000407/1-s2.0-S0002929712000407-main.pdf?_tid=9e02e0be-273c-11e2-8ec4-00000aab0f26&acdnat=1352115387_9b121eaf2f4d65b8ce34daed5d6fd017
NLM
Lines MA, Huang L, Schwartzentruber J, Douglas SL, Lynch DC, Beaulieu C, Guion-Almeida ML, Zechi-Ceide RM, Gener B, Gillessen-Kaesbach G, Nava C, Baujat G, Horn D, Kini U, Caliebe A, Alanay Y, Utine GE, Lev D, Kohlhase J, Grix AW, Lohmann DR, Hehr U, Böhm D, FORGE Canada Consortium, Majewski J, Bulman DE, Wieczorek D, Boycott KM. Haploinsufficiency of a spliceosomal GTPase encoded by EFTUD2 causes mandibulofacial dysostosis with microcephaly [Internet]. The American Journal of Human Genetics. 2012 ; 90( 2): 369-377.[citado 2025 out. 27 ] Available from: http://ac.els-cdn.com/S0002929712000407/1-s2.0-S0002929712000407-main.pdf?_tid=9e02e0be-273c-11e2-8ec4-00000aab0f26&acdnat=1352115387_9b121eaf2f4d65b8ce34daed5d6fd017
Vancouver
Lines MA, Huang L, Schwartzentruber J, Douglas SL, Lynch DC, Beaulieu C, Guion-Almeida ML, Zechi-Ceide RM, Gener B, Gillessen-Kaesbach G, Nava C, Baujat G, Horn D, Kini U, Caliebe A, Alanay Y, Utine GE, Lev D, Kohlhase J, Grix AW, Lohmann DR, Hehr U, Böhm D, FORGE Canada Consortium, Majewski J, Bulman DE, Wieczorek D, Boycott KM. Haploinsufficiency of a spliceosomal GTPase encoded by EFTUD2 causes mandibulofacial dysostosis with microcephaly [Internet]. The American Journal of Human Genetics. 2012 ; 90( 2): 369-377.[citado 2025 out. 27 ] Available from: http://ac.els-cdn.com/S0002929712000407/1-s2.0-S0002929712000407-main.pdf?_tid=9e02e0be-273c-11e2-8ec4-00000aab0f26&acdnat=1352115387_9b121eaf2f4d65b8ce34daed5d6fd017
Artigo de periodico
Consensus Statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies (2010)
Miller, David T.; Adam, Margaret P.; Aradhya, Swaroop; Biesecker, Leslie G.; Brothman, Arthur R.; Carter, Nigel P; Church, Deanna M.; Crolla, John, A; Eichler, E.; Epstein, Charles J; Faucett, W. Andrew; Feuk, Lars; Friedman, Jan M; Hamosh, Ada; Jackson, Laird; Kaminsky, Erin B.; Kok, Klaas; Krantz, Ian D.; Kuhn, Robert H; Lee, Charles; Ostell, James M.; Rosenberg, Carla ; Scherer, Stephen W; Spinner, Nancy B.; Stavropoulos, Dimitri J.; Tepperberg, James H.; Thorland, Erik C.; Vermeesch, Joris R; Waggoner, Darrel J.; Watson, Michael S.; Martin, Christa Lese; Ledbetter, David H.
Fonte: The American Journal of Human Genetics. Unidade: IB
Assuntos: DOENÇAS GENÉTICAS, DIAGNÓSTICO CLÍNICO
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MILLER, David T. et al. Consensus Statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies. The American Journal of Human Genetics, v. 86 n. 5, p. 749-764, 2010Tradução . . Disponível em: https://doi.org/10.1016/j.ajhg.2010.04.006. Acesso em: 27 out. 2025.
APA
Miller, D. T., Adam, M. P., Aradhya, S., Biesecker, L. G., Brothman, A. R., Carter, N. P., et al. (2010). Consensus Statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies. The American Journal of Human Genetics, 86 n. 5, 749-764. doi:10.1016/j.ajhg.2010.04.006
NLM
Miller DT, Adam MP, Aradhya S, Biesecker LG, Brothman AR, Carter NP, Church DM, Crolla J, Eichler E, Epstein CJ, Faucett WA, Feuk L, Friedman JM, Hamosh A, Jackson L, Kaminsky EB, Kok K, Krantz ID, Kuhn RH, Lee C, Ostell JM, Rosenberg C, Scherer SW, Spinner NB, Stavropoulos DJ, Tepperberg JH, Thorland EC, Vermeesch JR, Waggoner DJ, Watson MS, Martin CL, Ledbetter DH. Consensus Statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies [Internet]. The American Journal of Human Genetics. 2010 ; 86 n. 5 749-764.[citado 2025 out. 27 ] Available from: https://doi.org/10.1016/j.ajhg.2010.04.006
Vancouver
Miller DT, Adam MP, Aradhya S, Biesecker LG, Brothman AR, Carter NP, Church DM, Crolla J, Eichler E, Epstein CJ, Faucett WA, Feuk L, Friedman JM, Hamosh A, Jackson L, Kaminsky EB, Kok K, Krantz ID, Kuhn RH, Lee C, Ostell JM, Rosenberg C, Scherer SW, Spinner NB, Stavropoulos DJ, Tepperberg JH, Thorland EC, Vermeesch JR, Waggoner DJ, Watson MS, Martin CL, Ledbetter DH. Consensus Statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies [Internet]. The American Journal of Human Genetics. 2010 ; 86 n. 5 749-764.[citado 2025 out. 27 ] Available from: https://doi.org/10.1016/j.ajhg.2010.04.006
Trabalho de evento-resumo periodico
Discordant phenotypes in first cousins with UBE3A mutation (2002)
Morella, G. A.; Munoz, M. V. R.; Silva Júnior, W. A.; Wagstalf, J.; Pina Neto, João Monteiro de
Fonte: The American Journal of Human Genetics. Nome do evento: Annual Meeting of the American Society of Human Genetics. Unidade: FMRP
Assunto: GENÉTICA MÉDICA
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ABNT
MORELLA, G. A. et al. Discordant phenotypes in first cousins with UBE3A mutation. The American Journal of Human Genetics. Chicago: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. . Acesso em: 27 out. 2025. , 2002
APA
Morella, G. A., Munoz, M. V. R., Silva Júnior, W. A., Wagstalf, J., & Pina Neto, J. M. de. (2002). Discordant phenotypes in first cousins with UBE3A mutation. The American Journal of Human Genetics. Chicago: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo.
NLM
Morella GA, Munoz MVR, Silva Júnior WA, Wagstalf J, Pina Neto JM de. Discordant phenotypes in first cousins with UBE3A mutation. The American Journal of Human Genetics. 2002 ; 71 502 res. 1950.[citado 2025 out. 27 ]
Vancouver
Morella GA, Munoz MVR, Silva Júnior WA, Wagstalf J, Pina Neto JM de. Discordant phenotypes in first cousins with UBE3A mutation. The American Journal of Human Genetics. 2002 ; 71 502 res. 1950.[citado 2025 out. 27 ]
Trabalho de evento-resumo periodico
Expression of CTCF gene preimplantation embryos (2002)
Rios, A. F. L.; Fernandes, M. B.; Andrea, M. V.; Lôbo, Raysildo Barbosa; Mazucato, M.; Ramos, Ester Silveira
Fonte: The American Journal of Human Genetics. Nome do evento: Annual Meeting of the American Society of Human Genetics. Unidade: FMRP
Assunto: GENÉTICA MÉDICA
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ABNT
RIOS, A. F. L. et al. Expression of CTCF gene preimplantation embryos. The American Journal of Human Genetics. Chicago: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. . Acesso em: 27 out. 2025. , 2002
APA
Rios, A. F. L., Fernandes, M. B., Andrea, M. V., Lôbo, R. B., Mazucato, M., & Ramos, E. S. (2002). Expression of CTCF gene preimplantation embryos. The American Journal of Human Genetics. Chicago: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo.
NLM
Rios AFL, Fernandes MB, Andrea MV, Lôbo RB, Mazucato M, Ramos ES. Expression of CTCF gene preimplantation embryos. The American Journal of Human Genetics. 2002 ; 71 317 res. 847.[citado 2025 out. 27 ]
Vancouver
Rios AFL, Fernandes MB, Andrea MV, Lôbo RB, Mazucato M, Ramos ES. Expression of CTCF gene preimplantation embryos. The American Journal of Human Genetics. 2002 ; 71 317 res. 847.[citado 2025 out. 27 ]
Trabalho de evento-resumo periodico
Trisomy 17p resulting from isochromosome formation and whole arm translocation (2002)
Martinhago, C. D.; Souza, F. R. P.; Motta, V. M.; Nassar, A. C. C.; Laureano, L. A. F.; Ramos, Ester Silveira; Martelli, Lúcia Regina
Fonte: The American Journal of Human Genetics. Nome do evento: Annual Meeting of the American Society of Human Genetics. Unidade: FMRP
Assunto: GENÉTICA MÉDICA
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ABNT
MARTINHAGO, C. D. et al. Trisomy 17p resulting from isochromosome formation and whole arm translocation. The American Journal of Human Genetics. Chicago: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. . Acesso em: 27 out. 2025. , 2002
APA
Martinhago, C. D., Souza, F. R. P., Motta, V. M., Nassar, A. C. C., Laureano, L. A. F., Ramos, E. S., & Martelli, L. R. (2002). Trisomy 17p resulting from isochromosome formation and whole arm translocation. The American Journal of Human Genetics. Chicago: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo.
NLM
Martinhago CD, Souza FRP, Motta VM, Nassar ACC, Laureano LAF, Ramos ES, Martelli LR. Trisomy 17p resulting from isochromosome formation and whole arm translocation. The American Journal of Human Genetics. 2002 ; 71[citado 2025 out. 27 ]
Vancouver
Martinhago CD, Souza FRP, Motta VM, Nassar ACC, Laureano LAF, Ramos ES, Martelli LR. Trisomy 17p resulting from isochromosome formation and whole arm translocation. The American Journal of Human Genetics. 2002 ; 71[citado 2025 out. 27 ]
Trabalho de evento-resumo periodico
Mosaicismo for two different robertsonian translocations associated with infertility (2002)
Martelli, Lúcia Regina; Dentillo, D. B.; Cruzzi, J. F.; Santos, Sheila de Almeida; Ferreira, R. J.; Nassar, A. C. C.; Motta, V. M.; Ramos, Ester Silveira
Fonte: The American Journal of Human Genetics. Nome do evento: Annual Meeting of the American Society of Human Genetics. Unidade: FMRP
Assunto: GENÉTICA MÉDICA
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ABNT
MARTELLI, Lúcia Regina et al. Mosaicismo for two different robertsonian translocations associated with infertility. The American Journal of Human Genetics. Chicago: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. . Acesso em: 27 out. 2025. , 2002
APA
Martelli, L. R., Dentillo, D. B., Cruzzi, J. F., Santos, S. de A., Ferreira, R. J., Nassar, A. C. C., et al. (2002). Mosaicismo for two different robertsonian translocations associated with infertility. The American Journal of Human Genetics. Chicago: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo.
NLM
Martelli LR, Dentillo DB, Cruzzi JF, Santos S de A, Ferreira RJ, Nassar ACC, Motta VM, Ramos ES. Mosaicismo for two different robertsonian translocations associated with infertility. The American Journal of Human Genetics. 2002 ; 71 296 res. 729.[citado 2025 out. 27 ]
Vancouver
Martelli LR, Dentillo DB, Cruzzi JF, Santos S de A, Ferreira RJ, Nassar ACC, Motta VM, Ramos ES. Mosaicismo for two different robertsonian translocations associated with infertility. The American Journal of Human Genetics. 2002 ; 71 296 res. 729.[citado 2025 out. 27 ]
Trabalho de evento-resumo periodico
Preimplantation genetic diagnosis: attitudes and opinions (2002)
Ramos, Ester Silveira; Floria, Vicente M.; Bartmann, Ana Karina; Zambianchi, Ana Rosa; Martelli, Lúcia Regina
Fonte: The American Journal of Human Genetics. Nome do evento: Annual Meeting of the American Society of Human Genetics. Unidade: FMRP
Assunto: GENÉTICA MÉDICA
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ABNT
RAMOS, Ester Silveira et al. Preimplantation genetic diagnosis: attitudes and opinions. The American Journal of Human Genetics. Chicago: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. . Acesso em: 27 out. 2025. , 2002
APA
Ramos, E. S., Floria, V. M., Bartmann, A. K., Zambianchi, A. R., & Martelli, L. R. (2002). Preimplantation genetic diagnosis: attitudes and opinions. The American Journal of Human Genetics. Chicago: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo.
NLM
Ramos ES, Floria VM, Bartmann AK, Zambianchi AR, Martelli LR. Preimplantation genetic diagnosis: attitudes and opinions. The American Journal of Human Genetics. 2002 ; 71 345 res. 1010.[citado 2025 out. 27 ]
Vancouver
Ramos ES, Floria VM, Bartmann AK, Zambianchi AR, Martelli LR. Preimplantation genetic diagnosis: attitudes and opinions. The American Journal of Human Genetics. 2002 ; 71 345 res. 1010.[citado 2025 out. 27 ]
Trabalho de evento-resumo periodico
The effect of telethonin deficiency in LGMD-2G and its expression in other forms of muscular dystrophies and congenital myopathies (2000)
Vainzof, Mariz ; Moreira, E. S.; Passos-Bueno, Maria Rita ; Faulkner, Georgine; Valle, G.; Zanoteli, Edmar; Gurgel-Gianneti, Juliana; Ribeiro, Alberto de Freitas ; Silva, Helga Cristina Almeida da; Tsanaclis, Ana Maria Crous; Zatz, Mayana
Fonte: The American Journal of Human Genetics. Nome do evento: Annual Meeting of the American Society of Human Genetics. Unidades: IB, FM
Assunto: GENÉTICA MÉDICA
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ABNT
VAINZOF, Mariz et al. The effect of telethonin deficiency in LGMD-2G and its expression in other forms of muscular dystrophies and congenital myopathies. The American Journal of Human Genetics. Chicago: Instituto de Biociências, Universidade de São Paulo. . Acesso em: 27 out. 2025. , 2000
APA
Vainzof, M., Moreira, E. S., Passos-Bueno, M. R., Faulkner, G., Valle, G., Zanoteli, E., et al. (2000). The effect of telethonin deficiency in LGMD-2G and its expression in other forms of muscular dystrophies and congenital myopathies. The American Journal of Human Genetics. Chicago: Instituto de Biociências, Universidade de São Paulo.
NLM
Vainzof M, Moreira ES, Passos-Bueno MR, Faulkner G, Valle G, Zanoteli E, Gurgel-Gianneti J, Ribeiro A de F, Silva HCA da, Tsanaclis AMC, Zatz M. The effect of telethonin deficiency in LGMD-2G and its expression in other forms of muscular dystrophies and congenital myopathies. The American Journal of Human Genetics. 2000 ; 67( 4): 379.[citado 2025 out. 27 ]
Vancouver
Vainzof M, Moreira ES, Passos-Bueno MR, Faulkner G, Valle G, Zanoteli E, Gurgel-Gianneti J, Ribeiro A de F, Silva HCA da, Tsanaclis AMC, Zatz M. The effect of telethonin deficiency in LGMD-2G and its expression in other forms of muscular dystrophies and congenital myopathies. The American Journal of Human Genetics. 2000 ; 67( 4): 379.[citado 2025 out. 27 ]
Trabalho de evento-resumo periodico
Influence of CYP2E1 and GSTM1 polymorphism on the frequency of chromosome aberrations in lymphocytes of former alcoholics (1999)
Gattás, Gilka Jorge Fígaro; Calabrez, Mara Cristina Tramujas
Fonte: The American Journal of Human Genetics. Nome do evento: Annual Meeting of the American Society of Human Genetics by the University of Chicago. Unidade: FM
Assuntos: MEDICINA LEGAL, POLIMORFISMO
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ABNT
GATTÁS, Gilka Jorge Fígaro e CALABREZ, Mara Cristina Tramujas. Influence of CYP2E1 and GSTM1 polymorphism on the frequency of chromosome aberrations in lymphocytes of former alcoholics. The American Journal of Human Genetics. Chicago: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 27 out. 2025. , 1999
APA
Gattás, G. J. F., & Calabrez, M. C. T. (1999). Influence of CYP2E1 and GSTM1 polymorphism on the frequency of chromosome aberrations in lymphocytes of former alcoholics. The American Journal of Human Genetics. Chicago: Faculdade de Medicina, Universidade de São Paulo.
NLM
Gattás GJF, Calabrez MCT. Influence of CYP2E1 and GSTM1 polymorphism on the frequency of chromosome aberrations in lymphocytes of former alcoholics. The American Journal of Human Genetics. 1999 ; 65( 4): A163.[citado 2025 out. 27 ]
Vancouver
Gattás GJF, Calabrez MCT. Influence of CYP2E1 and GSTM1 polymorphism on the frequency of chromosome aberrations in lymphocytes of former alcoholics. The American Journal of Human Genetics. 1999 ; 65( 4): A163.[citado 2025 out. 27 ]
Trabalho de evento-resumo periodico
Analysis of the PTEN coding region in primary prostate carcinomas (1997)
Feilotter, Harriet E; Nagai, Maria Aparecida; Boag, Alexander H; Eng, Charis; Mulligan, Lois M
Fonte: The American Journal of Human Genetics. Nome do evento: The American Society of Human Genetics Annual Meeting. Unidade: FM
Assunto: MEDICINA INTERNA
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ABNT
FEILOTTER, Harriet E et al. Analysis of the PTEN coding region in primary prostate carcinomas. The American Journal of Human Genetics. Baltimore: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 27 out. 2025. , 1997
APA
Feilotter, H. E., Nagai, M. A., Boag, A. H., Eng, C., & Mulligan, L. M. (1997). Analysis of the PTEN coding region in primary prostate carcinomas. The American Journal of Human Genetics. Baltimore: Faculdade de Medicina, Universidade de São Paulo.
NLM
Feilotter HE, Nagai MA, Boag AH, Eng C, Mulligan LM. Analysis of the PTEN coding region in primary prostate carcinomas. The American Journal of Human Genetics. 1997 ; 61( 04): A65.[citado 2025 out. 27 ]
Vancouver
Feilotter HE, Nagai MA, Boag AH, Eng C, Mulligan LM. Analysis of the PTEN coding region in primary prostate carcinomas. The American Journal of Human Genetics. 1997 ; 61( 04): A65.[citado 2025 out. 27 ]
Trabalho de evento-resumo periodico
ATM mutations in sporadic breast cancer (1997)
Nagai, Maria Aparecida; Feilotter, H. E; Neto, M. M; Young, P. G; Mulligan, L. M
Fonte: The American Journal of Human Genetics. Nome do evento: The American Society of Human Genetics Annual Meeting. Unidade: FM
Assunto: MEDICINA INTERNA
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ABNT
NAGAI, Maria Aparecida et al. ATM mutations in sporadic breast cancer. The American Journal of Human Genetics. Baltimore: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 27 out. 2025. , 1997
APA
Nagai, M. A., Feilotter, H. E., Neto, M. M., Young, P. G., & Mulligan, L. M. (1997). ATM mutations in sporadic breast cancer. The American Journal of Human Genetics. Baltimore: Faculdade de Medicina, Universidade de São Paulo.
NLM
Nagai MA, Feilotter HE, Neto MM, Young PG, Mulligan LM. ATM mutations in sporadic breast cancer. The American Journal of Human Genetics. 1997 ; 61( 04): A76.[citado 2025 out. 27 ]
Vancouver
Nagai MA, Feilotter HE, Neto MM, Young PG, Mulligan LM. ATM mutations in sporadic breast cancer. The American Journal of Human Genetics. 1997 ; 61( 04): A76.[citado 2025 out. 27 ]

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