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Filtros : "Rosenberg, Carla" "Lisboa, Bianca Cristina Garcia" Limpar

Filtros

USP affiliated authors
- brentani, helena paula (2)
- rosenberg, carla (2)
- brentani, ricardo renzo (1)
- bueno, maria rita dos santos e passos (1)
- costa, silvia souza da (1)

Artigo de periodico
Integrative variation analysis reveals that a complex genotype may specify phenotype in siblings with Syndromic Autism Spectrum Disorder (2017)
Reis, Viviane Neri de Souza; Kitajima, João Paulo; Tahira, Ana Carolina; Feio-dos-Santos, Ana Cecília; Fock, Rodrigo Ambrosio; Lisboa, Bianca Cristina Garcia; Simões, Sérgio Nery; Krepischi, Ana Cristina Victorino ; Rosenberg, Carla ; Lourenço, Naila Cristina; Passos-Bueno, Maria Rita ; Brentani, Helena
Source: PLOS ONE. Unidades: IB, FM
Subjects: AUTISMO, ESPECTROS, SINAIS E SINTOMAS, DOENÇAS GENÉTICAS, GENÓTIPOS, FENÓTIPOS, TRANSTORNOS MENTAIS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
REIS, Viviane Neri de Souza et al. Integrative variation analysis reveals that a complex genotype may specify phenotype in siblings with Syndromic Autism Spectrum Disorder. PLOS ONE, v. 12, n. Ja 2017, p. 1-22, 2017Tradução . . Disponível em: https://doi.org/10.1371/journal.pone.0170386. Acesso em: 01 ago. 2024.
APA
Reis, V. N. de S., Kitajima, J. P., Tahira, A. C., Feio-dos-Santos, A. C., Fock, R. A., Lisboa, B. C. G., et al. (2017). Integrative variation analysis reveals that a complex genotype may specify phenotype in siblings with Syndromic Autism Spectrum Disorder. PLOS ONE, 12( Ja 2017), 1-22. doi:10.1371/journal.pone.0170386
NLM
Reis VN de S, Kitajima JP, Tahira AC, Feio-dos-Santos AC, Fock RA, Lisboa BCG, Simões SN, Krepischi ACV, Rosenberg C, Lourenço NC, Passos-Bueno MR, Brentani H. Integrative variation analysis reveals that a complex genotype may specify phenotype in siblings with Syndromic Autism Spectrum Disorder [Internet]. PLOS ONE. 2017 ; 12( Ja 2017): 1-22.[citado 2024 ago. 01 ] Available from: https://doi.org/10.1371/journal.pone.0170386
Vancouver
Reis VN de S, Kitajima JP, Tahira AC, Feio-dos-Santos AC, Fock RA, Lisboa BCG, Simões SN, Krepischi ACV, Rosenberg C, Lourenço NC, Passos-Bueno MR, Brentani H. Integrative variation analysis reveals that a complex genotype may specify phenotype in siblings with Syndromic Autism Spectrum Disorder [Internet]. PLOS ONE. 2017 ; 12( Ja 2017): 1-22.[citado 2024 ago. 01 ] Available from: https://doi.org/10.1371/journal.pone.0170386
Artigo de periodico
Germline DNA copy number variation in familial and early-onset breast cancer (2012)
Krepischi, Ana Cristina Victorino ; Achatz, Maria Izabel W; Santos, Erika Maria Monteiro; Costa, Sílvia S; Lisboa, Bianca Cristina Garcia; Brentani, Helena; Santos, Tiago M; Gonçalves, Amanda; Nóbrega, Amanda F; Pearson, Peter Lees; Vianna-Morgante, Angela M ; Carraro, Dirce M; Brentani, Ricardo Renzo; Rosenberg, Carla
Source: Breast Cancer Research. Unidades: IB, FM
Subjects: NEOPLASIAS MAMÁRIAS, GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
KREPISCHI, Ana Cristina Victorino et al. Germline DNA copy number variation in familial and early-onset breast cancer. Breast Cancer Research, v. 14, n. 1, p. R24-R31, 2012Tradução . . Disponível em: https://doi.org/10.1186/bcr3109. Acesso em: 01 ago. 2024.
APA
Krepischi, A. C. V., Achatz, M. I. W., Santos, E. M. M., Costa, S. S., Lisboa, B. C. G., Brentani, H., et al. (2012). Germline DNA copy number variation in familial and early-onset breast cancer. Breast Cancer Research, 14( 1), R24-R31. doi:10.1186/bcr3109
NLM
Krepischi ACV, Achatz MIW, Santos EMM, Costa SS, Lisboa BCG, Brentani H, Santos TM, Gonçalves A, Nóbrega AF, Pearson PL, Vianna-Morgante AM, Carraro DM, Brentani RR, Rosenberg C. Germline DNA copy number variation in familial and early-onset breast cancer [Internet]. Breast Cancer Research. 2012 ; 14( 1): R24-R31.[citado 2024 ago. 01 ] Available from: https://doi.org/10.1186/bcr3109
Vancouver
Krepischi ACV, Achatz MIW, Santos EMM, Costa SS, Lisboa BCG, Brentani H, Santos TM, Gonçalves A, Nóbrega AF, Pearson PL, Vianna-Morgante AM, Carraro DM, Brentani RR, Rosenberg C. Germline DNA copy number variation in familial and early-onset breast cancer [Internet]. Breast Cancer Research. 2012 ; 14( 1): R24-R31.[citado 2024 ago. 01 ] Available from: https://doi.org/10.1186/bcr3109

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