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Trabalho de evento-anais periodico
Fragile X polupation screening (2000)
MacPherson, James L.; Vianna-Morgante, Angela M
Source: American Journal of Medical Genetics. Conference titles: International Workshop on Fragile X Syndrome and X-Linked Mental Retardation. Unidade: IB
Subjects: ACONSELHAMENTO GENÉTICO, RETARDO MENTAL
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MACPHERSON, James L. e VIANNA-MORGANTE, Angela M. Fragile X polupation screening. American Journal of Medical Genetics. New York: Instituto de Biociências, Universidade de São Paulo. . Acesso em: 19 abr. 2024. , 2000
APA
MacPherson, J. L., & Vianna-Morgante, A. M. (2000). Fragile X polupation screening. American Journal of Medical Genetics. New York: Instituto de Biociências, Universidade de São Paulo.
NLM
MacPherson JL, Vianna-Morgante AM. Fragile X polupation screening. American Journal of Medical Genetics. 2000 ; 94( 5): 351-352.[citado 2024 abr. 19 ]
Vancouver
MacPherson JL, Vianna-Morgante AM. Fragile X polupation screening. American Journal of Medical Genetics. 2000 ; 94( 5): 351-352.[citado 2024 abr. 19 ]
Artigo de periodico
Mapping of the autosomal recessive (AR) craniometaphyseal dysplasia locus to chromosome region 6q21-22 and confirmation of genetic heterogeneity for mild AR spondylocostal dysplasia (2000)
Iughetti, Paula; Alonso, Luís Garcia; Wilcox, William; Alonso, Nivaldo
Source: American Journal of Medical Genetics. Unidade: IB
Assunto: GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
IUGHETTI, Paula et al. Mapping of the autosomal recessive (AR) craniometaphyseal dysplasia locus to chromosome region 6q21-22 and confirmation of genetic heterogeneity for mild AR spondylocostal dysplasia. American Journal of Medical Genetics, n. 95, p. 482-491, 2000Tradução . . Disponível em: https://doi.org/10.1002/1096-8628(20001218)95:5%3C482::aid-ajmg14%3E3.0.co;2-x. Acesso em: 19 abr. 2024.
APA
Iughetti, P., Alonso, L. G., Wilcox, W., & Alonso, N. (2000). Mapping of the autosomal recessive (AR) craniometaphyseal dysplasia locus to chromosome region 6q21-22 and confirmation of genetic heterogeneity for mild AR spondylocostal dysplasia. American Journal of Medical Genetics, ( 95), 482-491. doi:10.1002/1096-8628(20001218)95:5%3C482::aid-ajmg14%3E3.0.co;2-x
NLM
Iughetti P, Alonso LG, Wilcox W, Alonso N. Mapping of the autosomal recessive (AR) craniometaphyseal dysplasia locus to chromosome region 6q21-22 and confirmation of genetic heterogeneity for mild AR spondylocostal dysplasia [Internet]. American Journal of Medical Genetics. 2000 ;( 95): 482-491.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1002/1096-8628(20001218)95:5%3C482::aid-ajmg14%3E3.0.co;2-x
Vancouver
Iughetti P, Alonso LG, Wilcox W, Alonso N. Mapping of the autosomal recessive (AR) craniometaphyseal dysplasia locus to chromosome region 6q21-22 and confirmation of genetic heterogeneity for mild AR spondylocostal dysplasia [Internet]. American Journal of Medical Genetics. 2000 ;( 95): 482-491.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1002/1096-8628(20001218)95:5%3C482::aid-ajmg14%3E3.0.co;2-x
Artigo de periodico-carta/editorial
Neuroimaging and echocardiographic finding in sotos syndrome (2000)
Melo, Débora Gusmão; Pina Neto, João Monteiro de; Acosta, Angelina Xavier; Castro, José Daniel Vieira de; Santos, Antonio Carlos
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
MELO, Débora Gusmão et al. Neuroimaging and echocardiographic finding in sotos syndrome. American Journal of Medical Genetics. New York: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. . Acesso em: 19 abr. 2024. , 2000
APA
Melo, D. G., Pina Neto, J. M. de, Acosta, A. X., Castro, J. D. V. de, & Santos, A. C. (2000). Neuroimaging and echocardiographic finding in sotos syndrome. American Journal of Medical Genetics. New York: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo.
NLM
Melo DG, Pina Neto JM de, Acosta AX, Castro JDV de, Santos AC. Neuroimaging and echocardiographic finding in sotos syndrome. American Journal of Medical Genetics. 2000 ; 90 432-433.[citado 2024 abr. 19 ]
Vancouver
Melo DG, Pina Neto JM de, Acosta AX, Castro JDV de, Santos AC. Neuroimaging and echocardiographic finding in sotos syndrome. American Journal of Medical Genetics. 2000 ; 90 432-433.[citado 2024 abr. 19 ]
Artigo de periodico
Brazilian family with pure autosomal dominant spastic paraplegia maps to 8q: analysis of muscle beta 1 syntrophin (2000)
Rocco, P.; Vainzof, Mariz ; Froehner, S. C.; Peters, M. F.; Marie, Suely Kazue Nagahashi; Passos-Bueno, Maria Rita ; Zatz, Mayana
Source: American Journal of Medical Genetics. Unidades: FM, IB
Assunto: NEUROLOGIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ROCCO, P. et al. Brazilian family with pure autosomal dominant spastic paraplegia maps to 8q: analysis of muscle beta 1 syntrophin. American Journal of Medical Genetics, v. 92, p. 122-7, 2000Tradução . . Disponível em: https://doi.org/10.1002/(sici)1096-8628(20000515)92:2%3C122::aid-ajmg8%3E3.0.co;2-b. Acesso em: 19 abr. 2024.
APA
Rocco, P., Vainzof, M., Froehner, S. C., Peters, M. F., Marie, S. K. N., Passos-Bueno, M. R., & Zatz, M. (2000). Brazilian family with pure autosomal dominant spastic paraplegia maps to 8q: analysis of muscle beta 1 syntrophin. American Journal of Medical Genetics, 92, 122-7. doi:10.1002/(sici)1096-8628(20000515)92:2%3C122::aid-ajmg8%3E3.0.co;2-b
NLM
Rocco P, Vainzof M, Froehner SC, Peters MF, Marie SKN, Passos-Bueno MR, Zatz M. Brazilian family with pure autosomal dominant spastic paraplegia maps to 8q: analysis of muscle beta 1 syntrophin [Internet]. American Journal of Medical Genetics. 2000 ; 92 122-7.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1002/(sici)1096-8628(20000515)92:2%3C122::aid-ajmg8%3E3.0.co;2-b
Vancouver
Rocco P, Vainzof M, Froehner SC, Peters MF, Marie SKN, Passos-Bueno MR, Zatz M. Brazilian family with pure autosomal dominant spastic paraplegia maps to 8q: analysis of muscle beta 1 syntrophin [Internet]. American Journal of Medical Genetics. 2000 ; 92 122-7.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1002/(sici)1096-8628(20000515)92:2%3C122::aid-ajmg8%3E3.0.co;2-b
Artigo de periodico
"New" autosomal-dominant infantile sensorineural non-progressive high-frequency hearing loss: report on a Brazilian family (2000)
Zanchetta, Sthella; Ohara, Kouzaburo; Rodrigues, Patrícia T.; Carvalho, Ester L. L.; Richieri-Costa, Antonio
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
ZANCHETTA, Sthella et al. "New" autosomal-dominant infantile sensorineural non-progressive high-frequency hearing loss: report on a Brazilian family. American Journal of Medical Genetics, v. No 2000, n. 1, p. 13-16, 2000Tradução . . Disponível em: https://doi.org/10.1002/1096-8628(20001106)95:1%3C13::aid-ajmg4%3E3.0.co;2-t. Acesso em: 19 abr. 2024.
APA
Zanchetta, S., Ohara, K., Rodrigues, P. T., Carvalho, E. L. L., & Richieri-Costa, A. (2000). "New" autosomal-dominant infantile sensorineural non-progressive high-frequency hearing loss: report on a Brazilian family. American Journal of Medical Genetics, No 2000( 1), 13-16. doi:10.1002/1096-8628(20001106)95:1%3C13::aid-ajmg4%3E3.0.co;2-t
NLM
Zanchetta S, Ohara K, Rodrigues PT, Carvalho ELL, Richieri-Costa A. "New" autosomal-dominant infantile sensorineural non-progressive high-frequency hearing loss: report on a Brazilian family [Internet]. American Journal of Medical Genetics. 2000 ; No 2000( 1): 13-16.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1002/1096-8628(20001106)95:1%3C13::aid-ajmg4%3E3.0.co;2-t
Vancouver
Zanchetta S, Ohara K, Rodrigues PT, Carvalho ELL, Richieri-Costa A. "New" autosomal-dominant infantile sensorineural non-progressive high-frequency hearing loss: report on a Brazilian family [Internet]. American Journal of Medical Genetics. 2000 ; No 2000( 1): 13-16.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1002/1096-8628(20001106)95:1%3C13::aid-ajmg4%3E3.0.co;2-t
Artigo de periodico
Ablepharon-macrostomia syndrome: first report of familial ocurrence (2000)
Ferraz, Victor Evangelista de Faria; Melo, Débora G.; Hansing, Susanne E.
Source: American Journal of Medical Genetics. Unidade: FMRP
Subjects: OFTALMOPATIAS, GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
FERRAZ, Victor Evangelista de Faria e MELO, Débora G. e HANSING, Susanne E. Ablepharon-macrostomia syndrome: first report of familial ocurrence. American Journal of Medical Genetics, v. 94, p. 281-283, 2000Tradução . . Disponível em: https://doi.org/10.1002/1096-8628(20001002)94:4%3C281::aid-ajmg3%3E3.0.co;2-s. Acesso em: 19 abr. 2024.
APA
Ferraz, V. E. de F., Melo, D. G., & Hansing, S. E. (2000). Ablepharon-macrostomia syndrome: first report of familial ocurrence. American Journal of Medical Genetics, 94, 281-283. doi:10.1002/1096-8628(20001002)94:4%3C281::aid-ajmg3%3E3.0.co;2-s
NLM
Ferraz VE de F, Melo DG, Hansing SE. Ablepharon-macrostomia syndrome: first report of familial ocurrence [Internet]. American Journal of Medical Genetics. 2000 ; 94 281-283.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1002/1096-8628(20001002)94:4%3C281::aid-ajmg3%3E3.0.co;2-s
Vancouver
Ferraz VE de F, Melo DG, Hansing SE. Ablepharon-macrostomia syndrome: first report of familial ocurrence [Internet]. American Journal of Medical Genetics. 2000 ; 94 281-283.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1002/1096-8628(20001002)94:4%3C281::aid-ajmg3%3E3.0.co;2-s
Artigo de periodico
Heterozygosity probabilities for normal relatives of isolated cases affected by incompletely penetrant dominant conditions and the calculation of recurrence risks for their offspring: I. autosomal dominant genes (2000)
Otto, Paulo A ; Maestrelli, Sylvia Regina Pedrosa
Source: American Journal of Medical Genetics. Unidade: IB
Assunto: DOENÇAS GENÉTICAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
OTTO, Paulo A e MAESTRELLI, Sylvia Regina Pedrosa. Heterozygosity probabilities for normal relatives of isolated cases affected by incompletely penetrant dominant conditions and the calculation of recurrence risks for their offspring: I. autosomal dominant genes. American Journal of Medical Genetics, v. 95, n. 43-48, 2000Tradução . . Disponível em: https://doi.org/10.1002/1096-8628(20001106)95:1%3C43::aid-ajmg9%3E3.3.co;2-x. Acesso em: 19 abr. 2024.
APA
Otto, P. A., & Maestrelli, S. R. P. (2000). Heterozygosity probabilities for normal relatives of isolated cases affected by incompletely penetrant dominant conditions and the calculation of recurrence risks for their offspring: I. autosomal dominant genes. American Journal of Medical Genetics, 95( 43-48). doi:10.1002/1096-8628(20001106)95:1%3C43::aid-ajmg9%3E3.3.co;2-x
NLM
Otto PA, Maestrelli SRP. Heterozygosity probabilities for normal relatives of isolated cases affected by incompletely penetrant dominant conditions and the calculation of recurrence risks for their offspring: I. autosomal dominant genes [Internet]. American Journal of Medical Genetics. 2000 ; 95( 43-48):[citado 2024 abr. 19 ] Available from: https://doi.org/10.1002/1096-8628(20001106)95:1%3C43::aid-ajmg9%3E3.3.co;2-x
Vancouver
Otto PA, Maestrelli SRP. Heterozygosity probabilities for normal relatives of isolated cases affected by incompletely penetrant dominant conditions and the calculation of recurrence risks for their offspring: I. autosomal dominant genes [Internet]. American Journal of Medical Genetics. 2000 ; 95( 43-48):[citado 2024 abr. 19 ] Available from: https://doi.org/10.1002/1096-8628(20001106)95:1%3C43::aid-ajmg9%3E3.3.co;2-x
Artigo de periodico
Neuroimaging and echocardiographic findings in sotos syndrome (1999)
Melo, Débora Gusmão; Pina Neto, João Monteiro de; Acosta, Angelina Xavier; Castro, José Daniel Vieira de; Santos, Antonio Carlos
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
MELO, Débora Gusmão et al. Neuroimaging and echocardiographic findings in sotos syndrome. American Journal of Medical Genetics, v. 90, p. 1-2, 1999Tradução . . Disponível em: https://doi.org/10.1002/(sici)1096-8628(20000228)90:5%3C432::aid-ajmg15%3E3.0.co;2-d. Acesso em: 19 abr. 2024.
APA
Melo, D. G., Pina Neto, J. M. de, Acosta, A. X., Castro, J. D. V. de, & Santos, A. C. (1999). Neuroimaging and echocardiographic findings in sotos syndrome. American Journal of Medical Genetics, 90, 1-2. doi:10.1002/(sici)1096-8628(20000228)90:5%3C432::aid-ajmg15%3E3.0.co;2-d
NLM
Melo DG, Pina Neto JM de, Acosta AX, Castro JDV de, Santos AC. Neuroimaging and echocardiographic findings in sotos syndrome [Internet]. American Journal of Medical Genetics. 1999 ; 90 1-2.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1002/(sici)1096-8628(20000228)90:5%3C432::aid-ajmg15%3E3.0.co;2-d
Vancouver
Melo DG, Pina Neto JM de, Acosta AX, Castro JDV de, Santos AC. Neuroimaging and echocardiographic findings in sotos syndrome [Internet]. American Journal of Medical Genetics. 1999 ; 90 1-2.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1002/(sici)1096-8628(20000228)90:5%3C432::aid-ajmg15%3E3.0.co;2-d
Artigo de periodico
Multiple congenital anomalies syndrome: growth and mental retardation, microcephaly, preauricular skin tags, cleft palate, camptodactyly, and distal limb anomalies. Report on two unrelated Brazilian patients (1999)
Guion-Almeida, Maria Leine; Ceide, Roseli Maria Zechi; Richieri-Costa, Antonio
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
GUION-ALMEIDA, Maria Leine e CEIDE, Roseli Maria Zechi e RICHIERI-COSTA, Antonio. Multiple congenital anomalies syndrome: growth and mental retardation, microcephaly, preauricular skin tags, cleft palate, camptodactyly, and distal limb anomalies. Report on two unrelated Brazilian patients. American Journal of Medical Genetics, v. No 1999, n. 1, p. 72-77, 1999Tradução . . Disponível em: https://doi.org/10.1002/(sici)1096-8628(19991105)87:1%3C72::aid-ajmg15%3E3.0.co;2-7. Acesso em: 19 abr. 2024.
APA
Guion-Almeida, M. L., Ceide, R. M. Z., & Richieri-Costa, A. (1999). Multiple congenital anomalies syndrome: growth and mental retardation, microcephaly, preauricular skin tags, cleft palate, camptodactyly, and distal limb anomalies. Report on two unrelated Brazilian patients. American Journal of Medical Genetics, No 1999( 1), 72-77. doi:10.1002/(sici)1096-8628(19991105)87:1%3C72::aid-ajmg15%3E3.0.co;2-7
NLM
Guion-Almeida ML, Ceide RMZ, Richieri-Costa A. Multiple congenital anomalies syndrome: growth and mental retardation, microcephaly, preauricular skin tags, cleft palate, camptodactyly, and distal limb anomalies. Report on two unrelated Brazilian patients [Internet]. American Journal of Medical Genetics. 1999 ; No 1999( 1): 72-77.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1002/(sici)1096-8628(19991105)87:1%3C72::aid-ajmg15%3E3.0.co;2-7
Vancouver
Guion-Almeida ML, Ceide RMZ, Richieri-Costa A. Multiple congenital anomalies syndrome: growth and mental retardation, microcephaly, preauricular skin tags, cleft palate, camptodactyly, and distal limb anomalies. Report on two unrelated Brazilian patients [Internet]. American Journal of Medical Genetics. 1999 ; No 1999( 1): 72-77.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1002/(sici)1096-8628(19991105)87:1%3C72::aid-ajmg15%3E3.0.co;2-7
Artigo de periodico
Mandibulofacial dysostosis Bauru type syndrome: a new case (1999)
Ceide, Roseli Maria Zechi; 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
CEIDE, Roseli Maria Zechi e GUION-ALMEIDA, Maria Leine. Mandibulofacial dysostosis Bauru type syndrome: a new case. American Journal of Medical Genetics, v. 86, n. 2, p. 199-201, 1999Tradução . . Disponível em: https://doi.org/10.1002/(sici)1096-8628(19990910)86:2%3C199::aid-ajmg24%3E3.3.co;2-g. Acesso em: 19 abr. 2024.
APA
Ceide, R. M. Z., & Guion-Almeida, M. L. (1999). Mandibulofacial dysostosis Bauru type syndrome: a new case. American Journal of Medical Genetics, 86( 2), 199-201. doi:10.1002/(sici)1096-8628(19990910)86:2%3C199::aid-ajmg24%3E3.3.co;2-g
NLM
Ceide RMZ, Guion-Almeida ML. Mandibulofacial dysostosis Bauru type syndrome: a new case [Internet]. American Journal of Medical Genetics. 1999 ; 86( 2): 199-201.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1002/(sici)1096-8628(19990910)86:2%3C199::aid-ajmg24%3E3.3.co;2-g
Vancouver
Ceide RMZ, Guion-Almeida ML. Mandibulofacial dysostosis Bauru type syndrome: a new case [Internet]. American Journal of Medical Genetics. 1999 ; 86( 2): 199-201.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1002/(sici)1096-8628(19990910)86:2%3C199::aid-ajmg24%3E3.3.co;2-g
Artigo de periodico-carta/editorial
Role of the C677T Polymorphism at the MTHFR Gene on Risk to Nonsyndromic Cleft Lip With/Without Cleft Palate: results From a Case-Control Study in Brazil. [Carta] (1999)
Gaspar, D A; Pavanello, R.C; Zatz, Mayana ; Passos-Bueno, Maria Rita ; Andre, M; Steman, S; Wyszynski, D. F; Matioli, Sergio Russo
Source: American Journal of Medical Genetics. Unidade: IB
Subjects: GENÉTICA MÉDICA, LÁBIO FISSURADO, MUTAÇÃO GENÉTICA, POLIMORFISMO, MALFORMAÇÕES
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
GASPAR, D A et al. Role of the C677T Polymorphism at the MTHFR Gene on Risk to Nonsyndromic Cleft Lip With/Without Cleft Palate: results From a Case-Control Study in Brazil. [Carta]. American Journal of Medical Genetics. Hoboken: Instituto de Biociências, Universidade de São Paulo. Disponível em: https://doi.org/10.1002/(SICI)1096-8628(19991119)87:2%3C197::AID-AJMG15%3E3.0.CO;2-M. Acesso em: 19 abr. 2024. , 1999
APA
Gaspar, D. A., Pavanello, R. C., Zatz, M., Passos-Bueno, M. R., Andre, M., Steman, S., et al. (1999). Role of the C677T Polymorphism at the MTHFR Gene on Risk to Nonsyndromic Cleft Lip With/Without Cleft Palate: results From a Case-Control Study in Brazil. [Carta]. American Journal of Medical Genetics. Hoboken: Instituto de Biociências, Universidade de São Paulo. doi:10.1002/(SICI)1096-8628(19991119)87:2%3C197::AID-AJMG15%3E3.0.
NLM
Gaspar DA, Pavanello RC, Zatz M, Passos-Bueno MR, Andre M, Steman S, Wyszynski DF, Matioli SR. Role of the C677T Polymorphism at the MTHFR Gene on Risk to Nonsyndromic Cleft Lip With/Without Cleft Palate: results From a Case-Control Study in Brazil. [Carta] [Internet]. American Journal of Medical Genetics. 1999 ; 87 197-199.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1002/(SICI)1096-8628(19991119)87:2%3C197::AID-AJMG15%3E3.0.CO;2-M
Vancouver
Gaspar DA, Pavanello RC, Zatz M, Passos-Bueno MR, Andre M, Steman S, Wyszynski DF, Matioli SR. Role of the C677T Polymorphism at the MTHFR Gene on Risk to Nonsyndromic Cleft Lip With/Without Cleft Palate: results From a Case-Control Study in Brazil. [Carta] [Internet]. American Journal of Medical Genetics. 1999 ; 87 197-199.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1002/(SICI)1096-8628(19991119)87:2%3C197::AID-AJMG15%3E3.0.CO;2-M
Artigo de periodico
Holoprosencephaly in a Klinefelter fetus (1999)
Moraes, Edecio Armbruster; Shultz, Regina; Brizot, Maria de Lourdes; Miyadahira, Seizo; Zugaib, Marcelo
Source: American Journal of Medical Genetics. Unidade: FM
Assunto: OBSTETRÍCIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MORAES, Edecio Armbruster et al. Holoprosencephaly in a Klinefelter fetus. American Journal of Medical Genetics, v. 85, p. 511-512, 1999Tradução . . Disponível em: https://doi.org/10.1002/(sici)1096-8628(19990827)85:5%3C511::aid-ajmg15%3E3.0.co;2-s. Acesso em: 19 abr. 2024.
APA
Moraes, E. A., Shultz, R., Brizot, M. de L., Miyadahira, S., & Zugaib, M. (1999). Holoprosencephaly in a Klinefelter fetus. American Journal of Medical Genetics, 85, 511-512. doi:10.1002/(sici)1096-8628(19990827)85:5%3C511::aid-ajmg15%3E3.0.co;2-s
NLM
Moraes EA, Shultz R, Brizot M de L, Miyadahira S, Zugaib M. Holoprosencephaly in a Klinefelter fetus [Internet]. American Journal of Medical Genetics. 1999 ; 85 511-512.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1002/(sici)1096-8628(19990827)85:5%3C511::aid-ajmg15%3E3.0.co;2-s
Vancouver
Moraes EA, Shultz R, Brizot M de L, Miyadahira S, Zugaib M. Holoprosencephaly in a Klinefelter fetus [Internet]. American Journal of Medical Genetics. 1999 ; 85 511-512.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1002/(sici)1096-8628(19990827)85:5%3C511::aid-ajmg15%3E3.0.co;2-s
Artigo de periodico
DXS548/FRAXAC1 Haplotypes in fragile X chromosomes in the brazilian population (1999)
Mingroni Netto, Regina Celia ; Vianna-Morgante, Angela M ; Costa, Sílvia S; Angeli, Claudia Blanes
Source: American Journal of Medical Genetics. Unidade: IB
Assunto: GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MINGRONI NETTO, Regina Celia et al. DXS548/FRAXAC1 Haplotypes in fragile X chromosomes in the brazilian population. American Journal of Medical Genetics, v. 84, n. 3, p. 204-207, 1999Tradução . . Disponível em: https://doi.org/10.1002/(sici)1096-8628(19990528)84:3%3C204::aid-ajmg7%3E3.0.co;2-j. Acesso em: 19 abr. 2024.
APA
Mingroni Netto, R. C., Vianna-Morgante, A. M., Costa, S. S., & Angeli, C. B. (1999). DXS548/FRAXAC1 Haplotypes in fragile X chromosomes in the brazilian population. American Journal of Medical Genetics, 84( 3), 204-207. doi:10.1002/(sici)1096-8628(19990528)84:3%3C204::aid-ajmg7%3E3.0.co;2-j
NLM
Mingroni Netto RC, Vianna-Morgante AM, Costa SS, Angeli CB. DXS548/FRAXAC1 Haplotypes in fragile X chromosomes in the brazilian population [Internet]. American Journal of Medical Genetics. 1999 ;84( 3): 204-207.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1002/(sici)1096-8628(19990528)84:3%3C204::aid-ajmg7%3E3.0.co;2-j
Vancouver
Mingroni Netto RC, Vianna-Morgante AM, Costa SS, Angeli CB. DXS548/FRAXAC1 Haplotypes in fragile X chromosomes in the brazilian population [Internet]. American Journal of Medical Genetics. 1999 ;84( 3): 204-207.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1002/(sici)1096-8628(19990528)84:3%3C204::aid-ajmg7%3E3.0.co;2-j
Artigo de periodico
Fully mutated and Gray-zone FRAXA alleles in brazilian mentally retarded boys (1999)
Haddad, Luciana Amaral ; Mingroni Netto, Regina Celia ; Vianna-Morgante, Angela M ; Aguiar, Marcos J B; Costa, Sílvia S; Pena, Sérgio D J
Source: American Journal of Medical Genetics. Unidade: IB
Assunto: GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
HADDAD, Luciana Amaral et al. Fully mutated and Gray-zone FRAXA alleles in brazilian mentally retarded boys. American Journal of Medical Genetics, v. 84, n. 3, p. 198-201, 1999Tradução . . Disponível em: https://doi.org/10.1002/(sici)1096-8628(19990528)84:3%3C198::aid-ajmg5%3E3.0.co;2-w. Acesso em: 19 abr. 2024.
APA
Haddad, L. A., Mingroni Netto, R. C., Vianna-Morgante, A. M., Aguiar, M. J. B., Costa, S. S., & Pena, S. D. J. (1999). Fully mutated and Gray-zone FRAXA alleles in brazilian mentally retarded boys. American Journal of Medical Genetics, 84( 3), 198-201. doi:10.1002/(sici)1096-8628(19990528)84:3%3C198::aid-ajmg5%3E3.0.co;2-w
NLM
Haddad LA, Mingroni Netto RC, Vianna-Morgante AM, Aguiar MJB, Costa SS, Pena SDJ. Fully mutated and Gray-zone FRAXA alleles in brazilian mentally retarded boys [Internet]. American Journal of Medical Genetics. 1999 ; 84( 3): 198-201.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1002/(sici)1096-8628(19990528)84:3%3C198::aid-ajmg5%3E3.0.co;2-w
Vancouver
Haddad LA, Mingroni Netto RC, Vianna-Morgante AM, Aguiar MJB, Costa SS, Pena SDJ. Fully mutated and Gray-zone FRAXA alleles in brazilian mentally retarded boys [Internet]. American Journal of Medical Genetics. 1999 ; 84( 3): 198-201.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1002/(sici)1096-8628(19990528)84:3%3C198::aid-ajmg5%3E3.0.co;2-w
Artigo de periodico-carta/editorial
Screening of the C43G mutation in the promoter region of the XIST gene in females with highly skewed X-chromosome inactivation. [Carta] (1999)
Pereira, Lygia da Veiga ; Zatz, Mayana
Source: American Journal of Medical Genetics. Unidade: IB
Assunto: GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
PEREIRA, Lygia da Veiga e ZATZ, Mayana. Screening of the C43G mutation in the promoter region of the XIST gene in females with highly skewed X-chromosome inactivation. [Carta]. American Journal of Medical Genetics. New York: Instituto de Biociências, Universidade de São Paulo. . Acesso em: 19 abr. 2024. , 1999
APA
Pereira, L. da V., & Zatz, M. (1999). Screening of the C43G mutation in the promoter region of the XIST gene in females with highly skewed X-chromosome inactivation. [Carta]. American Journal of Medical Genetics. New York: Instituto de Biociências, Universidade de São Paulo.
NLM
Pereira L da V, Zatz M. Screening of the C43G mutation in the promoter region of the XIST gene in females with highly skewed X-chromosome inactivation. [Carta]. American Journal of Medical Genetics. 1999 ; 87 86-87.[citado 2024 abr. 19 ]
Vancouver
Pereira L da V, Zatz M. Screening of the C43G mutation in the promoter region of the XIST gene in females with highly skewed X-chromosome inactivation. [Carta]. American Journal of Medical Genetics. 1999 ; 87 86-87.[citado 2024 abr. 19 ]
Artigo de periodico
Lower lip pits and anorectal anomalies in Kabuki syndrome (1999)
Nakata, Nancy Mizue Kokitsu; Vendramini, Siulan; 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
NAKATA, Nancy Mizue Kokitsu e VENDRAMINI, Siulan e GUION-ALMEIDA, Maria Leine. Lower lip pits and anorectal anomalies in Kabuki syndrome. American Journal of Medical Genetics, v. 86, n. 3, p. 282-284, 1999Tradução . . Disponível em: https://doi.org/10.1002/(sici)1096-8628(19990917)86:3%3C282::aid-ajmg17%3E3.3.co;2-h. Acesso em: 19 abr. 2024.
APA
Nakata, N. M. K., Vendramini, S., & Guion-Almeida, M. L. (1999). Lower lip pits and anorectal anomalies in Kabuki syndrome. American Journal of Medical Genetics, 86( 3), 282-284. doi:10.1002/(sici)1096-8628(19990917)86:3%3C282::aid-ajmg17%3E3.3.co;2-h
NLM
Nakata NMK, Vendramini S, Guion-Almeida ML. Lower lip pits and anorectal anomalies in Kabuki syndrome [Internet]. American Journal of Medical Genetics. 1999 ; 86( 3): 282-284.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1002/(sici)1096-8628(19990917)86:3%3C282::aid-ajmg17%3E3.3.co;2-h
Vancouver
Nakata NMK, Vendramini S, Guion-Almeida ML. Lower lip pits and anorectal anomalies in Kabuki syndrome [Internet]. American Journal of Medical Genetics. 1999 ; 86( 3): 282-284.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1002/(sici)1096-8628(19990917)86:3%3C282::aid-ajmg17%3E3.3.co;2-h
Artigo de periodico
Auriculo-condylar syndrome: further evidence for a new disorder (1999)
Guion-Almeida, Maria Leine; Nakata, Nancy Mizue Kokitsu; Ceide, Roseli Maria Zechi; Vendramini, Siulan
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 et al. Auriculo-condylar syndrome: further evidence for a new disorder. American Journal of Medical Genetics, v. 86, n. 2, p. 130-133, 1999Tradução . . Disponível em: https://doi.org/10.1002/(sici)1096-8628(19990910)86:2%3C130::aid-ajmg8%3E3.3.co;2-f. Acesso em: 19 abr. 2024.
APA
Guion-Almeida, M. L., Nakata, N. M. K., Ceide, R. M. Z., & Vendramini, S. (1999). Auriculo-condylar syndrome: further evidence for a new disorder. American Journal of Medical Genetics, 86( 2), 130-133. doi:10.1002/(sici)1096-8628(19990910)86:2%3C130::aid-ajmg8%3E3.3.co;2-f
NLM
Guion-Almeida ML, Nakata NMK, Ceide RMZ, Vendramini S. Auriculo-condylar syndrome: further evidence for a new disorder [Internet]. American Journal of Medical Genetics. 1999 ; 86( 2): 130-133.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1002/(sici)1096-8628(19990910)86:2%3C130::aid-ajmg8%3E3.3.co;2-f
Vancouver
Guion-Almeida ML, Nakata NMK, Ceide RMZ, Vendramini S. Auriculo-condylar syndrome: further evidence for a new disorder [Internet]. American Journal of Medical Genetics. 1999 ; 86( 2): 130-133.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1002/(sici)1096-8628(19990910)86:2%3C130::aid-ajmg8%3E3.3.co;2-f
Artigo de periodico
Genetic counseling for childless women at risk for Duchenne muscular dystrophy (1999)
Eggers, Sabine; Pavanello, Rita de Cássia M.; Passos-Bueno, Maria Rita ; Zatz, Mayana
Source: American Journal of Medical Genetics. Unidade: IB
Subjects: GENÉTICA MÉDICA, DISTROFIA MUSCULAR
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
EGGERS, Sabine et al. Genetic counseling for childless women at risk for Duchenne muscular dystrophy. American Journal of Medical Genetics, v. 86, p. 447-453, 1999Tradução . . Disponível em: https://doi.org/10.1002/(sici)1096-8628(19991029)86:5%3C447::aid-ajmg10%3E3.0.co;2-p. Acesso em: 19 abr. 2024.
APA
Eggers, S., Pavanello, R. de C. M., Passos-Bueno, M. R., & Zatz, M. (1999). Genetic counseling for childless women at risk for Duchenne muscular dystrophy. American Journal of Medical Genetics, 86, 447-453. doi:10.1002/(sici)1096-8628(19991029)86:5%3C447::aid-ajmg10%3E3.0.co;2-p
NLM
Eggers S, Pavanello R de CM, Passos-Bueno MR, Zatz M. Genetic counseling for childless women at risk for Duchenne muscular dystrophy [Internet]. American Journal of Medical Genetics. 1999 ; 86 447-453.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1002/(sici)1096-8628(19991029)86:5%3C447::aid-ajmg10%3E3.0.co;2-p
Vancouver
Eggers S, Pavanello R de CM, Passos-Bueno MR, Zatz M. Genetic counseling for childless women at risk for Duchenne muscular dystrophy [Internet]. American Journal of Medical Genetics. 1999 ; 86 447-453.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1002/(sici)1096-8628(19991029)86:5%3C447::aid-ajmg10%3E3.0.co;2-p
Artigo de periodico
Seven autosomal recessive limb-girdle muscular dystrophies in the brazilian population: from LGMD2A to LGMD2G (1999)
Passos-Bueno, Maria Rita ; Vainzof, Mariz ; Moreira, Eloisa S.; Zatz, Mayana
Source: American Journal of Medical Genetics. Unidade: IB
Assunto: GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
PASSOS-BUENO, Maria Rita et al. Seven autosomal recessive limb-girdle muscular dystrophies in the brazilian population: from LGMD2A to LGMD2G. American Journal of Medical Genetics, v. 82, p. 392-398, 1999Tradução . . Disponível em: https://doi.org/10.1002/(sici)1096-8628(19990219)82:5%3C392::aid-ajmg7%3E3.0.co;2-0. Acesso em: 19 abr. 2024.
APA
Passos-Bueno, M. R., Vainzof, M., Moreira, E. S., & Zatz, M. (1999). Seven autosomal recessive limb-girdle muscular dystrophies in the brazilian population: from LGMD2A to LGMD2G. American Journal of Medical Genetics, 82, 392-398. doi:10.1002/(sici)1096-8628(19990219)82:5%3C392::aid-ajmg7%3E3.0.co;2-0
NLM
Passos-Bueno MR, Vainzof M, Moreira ES, Zatz M. Seven autosomal recessive limb-girdle muscular dystrophies in the brazilian population: from LGMD2A to LGMD2G [Internet]. American Journal of Medical Genetics. 1999 ; 82 392-398.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1002/(sici)1096-8628(19990219)82:5%3C392::aid-ajmg7%3E3.0.co;2-0
Vancouver
Passos-Bueno MR, Vainzof M, Moreira ES, Zatz M. Seven autosomal recessive limb-girdle muscular dystrophies in the brazilian population: from LGMD2A to LGMD2G [Internet]. American Journal of Medical Genetics. 1999 ; 82 392-398.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1002/(sici)1096-8628(19990219)82:5%3C392::aid-ajmg7%3E3.0.co;2-0
Artigo de periodico
New syndrome of growth and mental retardation, structural anomalies of the central nervous system, and first branchial arch, anophthalmia, heminasal a/hypoplasia, and atypical clefting: report on four Brazilian patients (1999)
Guion-Almeida, Maria Leine; Richieri-Costa, Antonio
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
GUION-ALMEIDA, Maria Leine e RICHIERI-COSTA, Antonio. New syndrome of growth and mental retardation, structural anomalies of the central nervous system, and first branchial arch, anophthalmia, heminasal a/hypoplasia, and atypical clefting: report on four Brazilian patients. American Journal of Medical Genetics, v. No 1999, n. 3, p. 237-244, 1999Tradução . . Disponível em: https://doi.org/10.1002/(sici)1096-8628(19991126)87:3%3C237::aid-ajmg8%3E3.0.co;2-i. Acesso em: 19 abr. 2024.
APA
Guion-Almeida, M. L., & Richieri-Costa, A. (1999). New syndrome of growth and mental retardation, structural anomalies of the central nervous system, and first branchial arch, anophthalmia, heminasal a/hypoplasia, and atypical clefting: report on four Brazilian patients. American Journal of Medical Genetics, No 1999( 3), 237-244. doi:10.1002/(sici)1096-8628(19991126)87:3%3C237::aid-ajmg8%3E3.0.co;2-i
NLM
Guion-Almeida ML, Richieri-Costa A. New syndrome of growth and mental retardation, structural anomalies of the central nervous system, and first branchial arch, anophthalmia, heminasal a/hypoplasia, and atypical clefting: report on four Brazilian patients [Internet]. American Journal of Medical Genetics. 1999 ; No 1999( 3): 237-244.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1002/(sici)1096-8628(19991126)87:3%3C237::aid-ajmg8%3E3.0.co;2-i
Vancouver
Guion-Almeida ML, Richieri-Costa A. New syndrome of growth and mental retardation, structural anomalies of the central nervous system, and first branchial arch, anophthalmia, heminasal a/hypoplasia, and atypical clefting: report on four Brazilian patients [Internet]. American Journal of Medical Genetics. 1999 ; No 1999( 3): 237-244.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1002/(sici)1096-8628(19991126)87:3%3C237::aid-ajmg8%3E3.0.co;2-i

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