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Artigo de periodico
Clinical characterization and underlying genetic findings in brazilian patients with syndromic microcephaly associated with neurodevelopmental disorders (2024)
Tolezano, Giovanna Cantini; Bastos, Giovanna Civitate; Costa, Silvia Souza da; Scliar, Marília de Oliveira; Souza, Carolina Fischinger Moura de; Linden Jr, Hélio Van Der; Fernandes, Walter Luiz Magalhães; Otto, Paulo A ; Vianna-Morgante, Angela M ; Haddad, Luciana Amaral ; Honjo, Rachel Sayuri; Yamamoto, Guilherme Lopes; Kim, Chong Ae; Rosenberg, Carla ; Jorge, Alexander Augusto de Lima ; Bertola, Débora Romeo ; Krepischi, Ana Cristina Victorino
Source: Molecular Neurobiology. Unidades: IB, BIOINFORMÁTICA, FM
Subjects: MICROCEFALIA, NEUROLOGIA, GENÉTICA
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ABNT
TOLEZANO, Giovanna Cantini et al. Clinical characterization and underlying genetic findings in brazilian patients with syndromic microcephaly associated with neurodevelopmental disorders. Molecular Neurobiology, 2024Tradução . . Disponível em: https://doi.org/10.1007/s12035-023-03894-8. Acesso em: 02 out. 2024.
APA
Tolezano, G. C., Bastos, G. C., Costa, S. S. da, Scliar, M. de O., Souza, C. F. M. de, Linden Jr, H. V. D., et al. (2024). Clinical characterization and underlying genetic findings in brazilian patients with syndromic microcephaly associated with neurodevelopmental disorders. Molecular Neurobiology. doi:10.1007/s12035-023-03894-8
NLM
Tolezano GC, Bastos GC, Costa SS da, Scliar M de O, Souza CFM de, Linden Jr HVD, Fernandes WLM, Otto PA, Vianna-Morgante AM, Haddad LA, Honjo RS, Yamamoto GL, Kim CA, Rosenberg C, Jorge AA de L, Bertola DR, Krepischi ACV. Clinical characterization and underlying genetic findings in brazilian patients with syndromic microcephaly associated with neurodevelopmental disorders [Internet]. Molecular Neurobiology. 2024 ;[citado 2024 out. 02 ] Available from: https://doi.org/10.1007/s12035-023-03894-8
Vancouver
Tolezano GC, Bastos GC, Costa SS da, Scliar M de O, Souza CFM de, Linden Jr HVD, Fernandes WLM, Otto PA, Vianna-Morgante AM, Haddad LA, Honjo RS, Yamamoto GL, Kim CA, Rosenberg C, Jorge AA de L, Bertola DR, Krepischi ACV. Clinical characterization and underlying genetic findings in brazilian patients with syndromic microcephaly associated with neurodevelopmental disorders [Internet]. Molecular Neurobiology. 2024 ;[citado 2024 out. 02 ] Available from: https://doi.org/10.1007/s12035-023-03894-8
Artigo de periodico
Skewed x-chromosome inactivation in women with idiopathic intellectual disability is indicative of pathogenic variants (2023)
Chaves, Luiza D; Carvalho, Laura M. L; Tolezano, Giovanna C; Pires, Sara F; Costa, Silvia S; Scliar, Marília O. de; Giuliani, Liane de R; Bertola, Débora Romeo ; Santos-Rebouças, Cíntia B; Seo, Go Hun; Otto, Paulo A ; Rosenberg, Carla ; Vianna-Morgante, Angela M ; Krepischi, Ana Cristina Victorino
Source: Molecular Neurobiology. Unidade: IB
Subjects: MULHERES, CROMOSSOMO X, RETARDO MENTAL, GENÉTICA MÉDICA
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ABNT
CHAVES, Luiza D et al. Skewed x-chromosome inactivation in women with idiopathic intellectual disability is indicative of pathogenic variants. Molecular Neurobiology, v. 60, p. 3758–3769, 2023Tradução . . Disponível em: https://doi.org/10.1007/s12035-023-03311-0. Acesso em: 02 out. 2024.
APA
Chaves, L. D., Carvalho, L. M. L., Tolezano, G. C., Pires, S. F., Costa, S. S., Scliar, M. O. de, et al. (2023). Skewed x-chromosome inactivation in women with idiopathic intellectual disability is indicative of pathogenic variants. Molecular Neurobiology, 60, 3758–3769. doi:10.1007/s12035-023-03311-0
NLM
Chaves LD, Carvalho LML, Tolezano GC, Pires SF, Costa SS, Scliar MO de, Giuliani L de R, Bertola DR, Santos-Rebouças CB, Seo GH, Otto PA, Rosenberg C, Vianna-Morgante AM, Krepischi ACV. Skewed x-chromosome inactivation in women with idiopathic intellectual disability is indicative of pathogenic variants [Internet]. Molecular Neurobiology. 2023 ; 60 3758–3769.[citado 2024 out. 02 ] Available from: https://doi.org/10.1007/s12035-023-03311-0
Vancouver
Chaves LD, Carvalho LML, Tolezano GC, Pires SF, Costa SS, Scliar MO de, Giuliani L de R, Bertola DR, Santos-Rebouças CB, Seo GH, Otto PA, Rosenberg C, Vianna-Morgante AM, Krepischi ACV. Skewed x-chromosome inactivation in women with idiopathic intellectual disability is indicative of pathogenic variants [Internet]. Molecular Neurobiology. 2023 ; 60 3758–3769.[citado 2024 out. 02 ] Available from: https://doi.org/10.1007/s12035-023-03311-0
Artigo de periodico
Burden of rare copy number variants in microcephaly: a Brazilian cohort of 185 microcephalic patients and review of the literature (2022)
Tolezano, Giovanna Cantini; Bastos, Giovanna Civitate; Costa, Silvia Souza da; Freire, Bruna Lucheze; Homma, Thais Kataoka; Honjo, Rachel Sayuri ; Yamamoto, Guilherme Lopes ; Passos-Bueno, Maria Rita ; Koiffmann, Celia Priszkulnik ; Kim, Chong Ae ; Vianna-Morgante, Angela M ; Jorge, Alexander Augusto de Lima ; Bertola, Débora Romeo ; Rosenberg, Carla ; Krepischi, Ana Cristina Victorino
Source: Journal of Autism and Developmental Disorders. Unidades: IB, FM
Subjects: MICROCEFALIA, REVISÃO SISTEMÁTICA
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ABNT
TOLEZANO, Giovanna Cantini et al. Burden of rare copy number variants in microcephaly: a Brazilian cohort of 185 microcephalic patients and review of the literature. Journal of Autism and Developmental Disorders, 2022Tradução . . Disponível em: https://doi.org/10.1007/s10803-022-05853-z. Acesso em: 02 out. 2024.
APA
Tolezano, G. C., Bastos, G. C., Costa, S. S. da, Freire, B. L., Homma, T. K., Honjo, R. S., et al. (2022). Burden of rare copy number variants in microcephaly: a Brazilian cohort of 185 microcephalic patients and review of the literature. Journal of Autism and Developmental Disorders. doi:10.1007/s10803-022-05853-z
NLM
Tolezano GC, Bastos GC, Costa SS da, Freire BL, Homma TK, Honjo RS, Yamamoto GL, Passos-Bueno MR, Koiffmann CP, Kim CA, Vianna-Morgante AM, Jorge AA de L, Bertola DR, Rosenberg C, Krepischi ACV. Burden of rare copy number variants in microcephaly: a Brazilian cohort of 185 microcephalic patients and review of the literature [Internet]. Journal of Autism and Developmental Disorders. 2022 ;[citado 2024 out. 02 ] Available from: https://doi.org/10.1007/s10803-022-05853-z
Vancouver
Tolezano GC, Bastos GC, Costa SS da, Freire BL, Homma TK, Honjo RS, Yamamoto GL, Passos-Bueno MR, Koiffmann CP, Kim CA, Vianna-Morgante AM, Jorge AA de L, Bertola DR, Rosenberg C, Krepischi ACV. Burden of rare copy number variants in microcephaly: a Brazilian cohort of 185 microcephalic patients and review of the literature [Internet]. Journal of Autism and Developmental Disorders. 2022 ;[citado 2024 out. 02 ] Available from: https://doi.org/10.1007/s10803-022-05853-z
Artigo de periodico
Microduplication of the ICR2 domain at chromosome 11p15 and familial Silver–Russell syndrome (2011)
Bonaldi, Adriano; Mazzeu, Juliana Forte; Costa, Silvia Souza da; Honjo, Rachel Sayuri; Bertola, Débora Romeo; Albano, Lilian Maria José; Furquim, Isabel M; Kim, Chong A; Vianna-Morgante, Angela M
Source: American Journal of Medical Genetics Part A. Unidade: IB
Subjects: DOENÇAS GENÉTICAS, EXPRESSÃO GÊNICA, ANORMALIDADES CROMOSSÔMICAS
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ABNT
BONALDI, Adriano et al. Microduplication of the ICR2 domain at chromosome 11p15 and familial Silver–Russell syndrome. American Journal of Medical Genetics Part A, v. 155, n. 10, p. 2479-2483, 2011Tradução . . Disponível em: https://doi.org/10.1002/ajmg.a.34023. Acesso em: 02 out. 2024.
APA
Bonaldi, A., Mazzeu, J. F., Costa, S. S. da, Honjo, R. S., Bertola, D. R., Albano, L. M. J., et al. (2011). Microduplication of the ICR2 domain at chromosome 11p15 and familial Silver–Russell syndrome. American Journal of Medical Genetics Part A, 155( 10), 2479-2483. doi:10.1002/ajmg.a.34023
NLM
Bonaldi A, Mazzeu JF, Costa SS da, Honjo RS, Bertola DR, Albano LMJ, Furquim IM, Kim CA, Vianna-Morgante AM. Microduplication of the ICR2 domain at chromosome 11p15 and familial Silver–Russell syndrome [Internet]. American Journal of Medical Genetics Part A. 2011 ; 155( 10): 2479-2483.[citado 2024 out. 02 ] Available from: https://doi.org/10.1002/ajmg.a.34023
Vancouver
Bonaldi A, Mazzeu JF, Costa SS da, Honjo RS, Bertola DR, Albano LMJ, Furquim IM, Kim CA, Vianna-Morgante AM. Microduplication of the ICR2 domain at chromosome 11p15 and familial Silver–Russell syndrome [Internet]. American Journal of Medical Genetics Part A. 2011 ; 155( 10): 2479-2483.[citado 2024 out. 02 ] Available from: https://doi.org/10.1002/ajmg.a.34023
Artigo de periodico
An illustrative case of neurofibromatosis type 1 and NF1 microdeletion (2010)
Praxedes, Leide de Almeida; Pereira, Flávia Moutinho; Mazzeu, Juliana Forte; Costa, Silvia Souza da; Bertola, Débora Romeo; Kim, Chong Ae; Vianna-Morgante, Angela M ; Otto, Paulo A
Source: Molecular Syndromology. Unidade: IB
Subjects: NEUROFIBROMATOSES, GENÉTICA MÉDICA
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ABNT
PRAXEDES, Leide de Almeida et al. An illustrative case of neurofibromatosis type 1 and NF1 microdeletion. Molecular Syndromology, v. 1, n. 3, p. 133-135, 2010Tradução . . Acesso em: 02 out. 2024.
APA
Praxedes, L. de A., Pereira, F. M., Mazzeu, J. F., Costa, S. S. da, Bertola, D. R., Kim, C. A., et al. (2010). An illustrative case of neurofibromatosis type 1 and NF1 microdeletion. Molecular Syndromology, 1( 3), 133-135.
NLM
Praxedes L de A, Pereira FM, Mazzeu JF, Costa SS da, Bertola DR, Kim CA, Vianna-Morgante AM, Otto PA. An illustrative case of neurofibromatosis type 1 and NF1 microdeletion. Molecular Syndromology. 2010 ; 1( 3): 133-135.[citado 2024 out. 02 ]
Vancouver
Praxedes L de A, Pereira FM, Mazzeu JF, Costa SS da, Bertola DR, Kim CA, Vianna-Morgante AM, Otto PA. An illustrative case of neurofibromatosis type 1 and NF1 microdeletion. Molecular Syndromology. 2010 ; 1( 3): 133-135.[citado 2024 out. 02 ]
Trabalho de evento-resumo
2q24.2 microdeletions encompassing the SLC4A10 gene are associated with idiopathic epilepsy and mental impairment (2009)
Krepischi, Ana Cristina Victorino ; Knijnenburg, Jeroen; Bertola, Débora Romeo; Kim, Chong Ae; Kok, Fernando; Vianna-Morgante, Angela M ; Rosenberg, Carla
Source: Abstracts. Conference titles: International Workshop on Fragile X and X-Linked Mental Retardation. Unidade: IB
Assunto: RETARDO MENTAL
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ABNT
KREPISCHI, Ana Cristina Victorino et al. 2q24.2 microdeletions encompassing the SLC4A10 gene are associated with idiopathic epilepsy and mental impairment. 2009, Anais.. Salvador: Instituto de Biociências, Universidade de São Paulo, 2009. . Acesso em: 02 out. 2024.
APA
Krepischi, A. C. V., Knijnenburg, J., Bertola, D. R., Kim, C. A., Kok, F., Vianna-Morgante, A. M., & Rosenberg, C. (2009). 2q24.2 microdeletions encompassing the SLC4A10 gene are associated with idiopathic epilepsy and mental impairment. In Abstracts. Salvador: Instituto de Biociências, Universidade de São Paulo.
NLM
Krepischi ACV, Knijnenburg J, Bertola DR, Kim CA, Kok F, Vianna-Morgante AM, Rosenberg C. 2q24.2 microdeletions encompassing the SLC4A10 gene are associated with idiopathic epilepsy and mental impairment. Abstracts. 2009 ;[citado 2024 out. 02 ]
Vancouver
Krepischi ACV, Knijnenburg J, Bertola DR, Kim CA, Kok F, Vianna-Morgante AM, Rosenberg C. 2q24.2 microdeletions encompassing the SLC4A10 gene are associated with idiopathic epilepsy and mental impairment. Abstracts. 2009 ;[citado 2024 out. 02 ]
Trabalho de evento-resumo
Microduplication at 11p15 in a family with five children affected by Silver-Russel syndrome provides further evidence of ICR2 involvement in the syndrome (2009)
Bonaldi, A.; Mazzeu, Juliana Forte; Honjo, Rachel Sayuri; Bertola, Débora Romeo; Albano, Lilian Maria José; Furquim, I. M.; Kim, C. A.; Vianna-Morgante, Angela M
Source: Resumo. Conference titles: Congresso Brasileiro de Genética. Unidade: IB
Assunto: ANORMALIDADES CROMOSSÔMICAS
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ABNT
BONALDI, A. et al. Microduplication at 11p15 in a family with five children affected by Silver-Russel syndrome provides further evidence of ICR2 involvement in the syndrome. 2009, Anais.. Águas de Lindóia: Instituto de Biociências, Universidade de São Paulo, 2009. . Acesso em: 02 out. 2024.
APA
Bonaldi, A., Mazzeu, J. F., Honjo, R. S., Bertola, D. R., Albano, L. M. J., Furquim, I. M., et al. (2009). Microduplication at 11p15 in a family with five children affected by Silver-Russel syndrome provides further evidence of ICR2 involvement in the syndrome. In Resumo. Águas de Lindóia: Instituto de Biociências, Universidade de São Paulo.
NLM
Bonaldi A, Mazzeu JF, Honjo RS, Bertola DR, Albano LMJ, Furquim IM, Kim CA, Vianna-Morgante AM. Microduplication at 11p15 in a family with five children affected by Silver-Russel syndrome provides further evidence of ICR2 involvement in the syndrome. Resumo. 2009 ;[citado 2024 out. 02 ]
Vancouver
Bonaldi A, Mazzeu JF, Honjo RS, Bertola DR, Albano LMJ, Furquim IM, Kim CA, Vianna-Morgante AM. Microduplication at 11p15 in a family with five children affected by Silver-Russel syndrome provides further evidence of ICR2 involvement in the syndrome. Resumo. 2009 ;[citado 2024 out. 02 ]
Artigo de periodico
High frequency of submicroscopic chromosomal imbalances in patients with syndromic craniosynostosis detected by a combined approach of microsatellite segregation analysis, multiplex ligation-dependent probe amplification and array-based comparative genome hybridisation (2008)
Jehee, Fernanda Sarquis; Krepischi, Ana Cristina Victorino ; Rocha, K. M.; Cavalcanti, D. P.; Kim, C. A.; Bertola, Débora Romeo; Alonso, Luís Garcia; D'Angelo, C. S.; Mazzeu, Juliana Forte; Froyen, Guy; Lugtenberg, D.; Vianna-Morgante, Angela M ; Rosenberg, Carla ; Passos-Bueno, Maria Rita
Source: Journal of Medical Genetics. Unidade: IB
Subjects: CRANIOSSINOSTOSE, ANORMALIDADES CRANIOFACIAIS
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ABNT
JEHEE, Fernanda Sarquis et al. High frequency of submicroscopic chromosomal imbalances in patients with syndromic craniosynostosis detected by a combined approach of microsatellite segregation analysis, multiplex ligation-dependent probe amplification and array-based comparative genome hybridisation. Journal of Medical Genetics, v. 45, n. 7, p. 447-450, 2008Tradução . . Disponível em: https://doi.org/10.1136/jmg.2007.057042. Acesso em: 02 out. 2024.
APA
Jehee, F. S., Krepischi, A. C. V., Rocha, K. M., Cavalcanti, D. P., Kim, C. A., Bertola, D. R., et al. (2008). High frequency of submicroscopic chromosomal imbalances in patients with syndromic craniosynostosis detected by a combined approach of microsatellite segregation analysis, multiplex ligation-dependent probe amplification and array-based comparative genome hybridisation. Journal of Medical Genetics, 45( 7), 447-450. doi:10.1136/jmg.2007.057042
NLM
Jehee FS, Krepischi ACV, Rocha KM, Cavalcanti DP, Kim CA, Bertola DR, Alonso LG, D'Angelo CS, Mazzeu JF, Froyen G, Lugtenberg D, Vianna-Morgante AM, Rosenberg C, Passos-Bueno MR. High frequency of submicroscopic chromosomal imbalances in patients with syndromic craniosynostosis detected by a combined approach of microsatellite segregation analysis, multiplex ligation-dependent probe amplification and array-based comparative genome hybridisation [Internet]. Journal of Medical Genetics. 2008 ; 45( 7): 447-450.[citado 2024 out. 02 ] Available from: https://doi.org/10.1136/jmg.2007.057042
Vancouver
Jehee FS, Krepischi ACV, Rocha KM, Cavalcanti DP, Kim CA, Bertola DR, Alonso LG, D'Angelo CS, Mazzeu JF, Froyen G, Lugtenberg D, Vianna-Morgante AM, Rosenberg C, Passos-Bueno MR. High frequency of submicroscopic chromosomal imbalances in patients with syndromic craniosynostosis detected by a combined approach of microsatellite segregation analysis, multiplex ligation-dependent probe amplification and array-based comparative genome hybridisation [Internet]. Journal of Medical Genetics. 2008 ; 45( 7): 447-450.[citado 2024 out. 02 ] Available from: https://doi.org/10.1136/jmg.2007.057042
Trabalho de evento-resumo
Duplication restricted to ICR2 (KCNQ1, KCNQ1OT1 genes) at 11p15 segregating in a family with five children affected by Silver-Russel syndrome (2008)
Vianna-Morgante, Angela M ; Bonaldi, A.; Honjo, Rachel Sayuri; Bertola, Débora Romeo; Albano, Lilian Maria José; Furquim, I. M.; Kim, C. A.; Mazzeu, Juliana Forte
Source: Resumo. Conference titles: Annual Meeting of the American Society of Human Genetics. Unidade: IB
Assunto: ANORMALIDADES CROMOSSÔMICAS
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ABNT
VIANNA-MORGANTE, Angela M et al. Duplication restricted to ICR2 (KCNQ1, KCNQ1OT1 genes) at 11p15 segregating in a family with five children affected by Silver-Russel syndrome. 2008, Anais.. Philadelphia: Instituto de Biociências, Universidade de São Paulo, 2008. . Acesso em: 02 out. 2024.
APA
Vianna-Morgante, A. M., Bonaldi, A., Honjo, R. S., Bertola, D. R., Albano, L. M. J., Furquim, I. M., et al. (2008). Duplication restricted to ICR2 (KCNQ1, KCNQ1OT1 genes) at 11p15 segregating in a family with five children affected by Silver-Russel syndrome. In Resumo. Philadelphia: Instituto de Biociências, Universidade de São Paulo.
NLM
Vianna-Morgante AM, Bonaldi A, Honjo RS, Bertola DR, Albano LMJ, Furquim IM, Kim CA, Mazzeu JF. Duplication restricted to ICR2 (KCNQ1, KCNQ1OT1 genes) at 11p15 segregating in a family with five children affected by Silver-Russel syndrome. Resumo. 2008 ;[citado 2024 out. 02 ]
Vancouver
Vianna-Morgante AM, Bonaldi A, Honjo RS, Bertola DR, Albano LMJ, Furquim IM, Kim CA, Mazzeu JF. Duplication restricted to ICR2 (KCNQ1, KCNQ1OT1 genes) at 11p15 segregating in a family with five children affected by Silver-Russel syndrome. Resumo. 2008 ;[citado 2024 out. 02 ]
Artigo de periodico
An 11q11-q13.3 duplication, including FGF3 and FGF4 genes, in a patient with syndromic multiple craniosynostoses (2007)
Jehee, Fernanda Sarquis; Bertola, Débora Romeo; Yelavarthi, Krishan K.; Krepischi, Ana Cristina Victorino ; Kim, Chong; Vianna-Morgante, Angela M ; Vermeesch, Joris R.; Passos-Bueno, Maria Rita
Source: American Journal of Medical Genetics. Part A. Unidade: IB
Subjects: CRANIOSSINOSTOSE, ANORMALIDADES CROMOSSÔMICAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
JEHEE, Fernanda Sarquis et al. An 11q11-q13.3 duplication, including FGF3 and FGF4 genes, in a patient with syndromic multiple craniosynostoses. American Journal of Medical Genetics. Part A, v. 143A, n. 16, p. 1912-1918, 2007Tradução . . Disponível em: https://doi.org/10.1002/ajmg.a.31863. Acesso em: 02 out. 2024.
APA
Jehee, F. S., Bertola, D. R., Yelavarthi, K. K., Krepischi, A. C. V., Kim, C., Vianna-Morgante, A. M., et al. (2007). An 11q11-q13.3 duplication, including FGF3 and FGF4 genes, in a patient with syndromic multiple craniosynostoses. American Journal of Medical Genetics. Part A, 143A( 16), 1912-1918. doi:10.1002/ajmg.a.31863
NLM
Jehee FS, Bertola DR, Yelavarthi KK, Krepischi ACV, Kim C, Vianna-Morgante AM, Vermeesch JR, Passos-Bueno MR. An 11q11-q13.3 duplication, including FGF3 and FGF4 genes, in a patient with syndromic multiple craniosynostoses [Internet]. American Journal of Medical Genetics. Part A. 2007 ; 143A( 16): 1912-1918.[citado 2024 out. 02 ] Available from: https://doi.org/10.1002/ajmg.a.31863
Vancouver
Jehee FS, Bertola DR, Yelavarthi KK, Krepischi ACV, Kim C, Vianna-Morgante AM, Vermeesch JR, Passos-Bueno MR. An 11q11-q13.3 duplication, including FGF3 and FGF4 genes, in a patient with syndromic multiple craniosynostoses [Internet]. American Journal of Medical Genetics. Part A. 2007 ; 143A( 16): 1912-1918.[citado 2024 out. 02 ] Available from: https://doi.org/10.1002/ajmg.a.31863
Artigo de periodico
Whole-genome array-CGH screening in undiagnosed syndromic patients: old syndromes revisited and new alterations (2006)
Krepischi, Ana Cristina Victorino ; Vianna-Morgante, Angela M ; Jehee, Fernanda Sarquis; Passos-Bueno, Maria Rita ; Knijnenburg, Jeroen; Szuhai, K.; Sloos, W.; Mazzeu, Juliana Forte; Kok, Fernando; Cheroki, C.; Otto, Paulo A ; Mingroni Netto, Regina Celia ; Varela, Monica Castro; Koiffmann, Celia Priszkulnik ; Kim, Chong A.; Bertola, Débora Romeo; Pearson, Peter Lees
Source: Cytogenetic and Genome Research. Unidade: IB
Assunto: ANORMALIDADES CROMOSSÔMICAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
KREPISCHI, Ana Cristina Victorino et al. Whole-genome array-CGH screening in undiagnosed syndromic patients: old syndromes revisited and new alterations. Cytogenetic and Genome Research, v. 115, n. 3-4, p. 254-261, 2006Tradução . . Disponível em: https://doi.org/10.1159/000095922. Acesso em: 02 out. 2024.
APA
Krepischi, A. C. V., Vianna-Morgante, A. M., Jehee, F. S., Passos-Bueno, M. R., Knijnenburg, J., Szuhai, K., et al. (2006). Whole-genome array-CGH screening in undiagnosed syndromic patients: old syndromes revisited and new alterations. Cytogenetic and Genome Research, 115( 3-4), 254-261. doi:10.1159/000095922
NLM
Krepischi ACV, Vianna-Morgante AM, Jehee FS, Passos-Bueno MR, Knijnenburg J, Szuhai K, Sloos W, Mazzeu JF, Kok F, Cheroki C, Otto PA, Mingroni Netto RC, Varela MC, Koiffmann CP, Kim CA, Bertola DR, Pearson PL. Whole-genome array-CGH screening in undiagnosed syndromic patients: old syndromes revisited and new alterations [Internet]. Cytogenetic and Genome Research. 2006 ; 115( 3-4): 254-261.[citado 2024 out. 02 ] Available from: https://doi.org/10.1159/000095922
Vancouver
Krepischi ACV, Vianna-Morgante AM, Jehee FS, Passos-Bueno MR, Knijnenburg J, Szuhai K, Sloos W, Mazzeu JF, Kok F, Cheroki C, Otto PA, Mingroni Netto RC, Varela MC, Koiffmann CP, Kim CA, Bertola DR, Pearson PL. Whole-genome array-CGH screening in undiagnosed syndromic patients: old syndromes revisited and new alterations [Internet]. Cytogenetic and Genome Research. 2006 ; 115( 3-4): 254-261.[citado 2024 out. 02 ] Available from: https://doi.org/10.1159/000095922

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