ReP USP - Resultado da busca

Filtros : "ZATZ, MAYANA" "ALONSO, NIVALDO" Removidos: "Department of Statistics, Universidade Estadual da Paraíba (UEPB), Campina Grande" "Zoboli, Elma Lourdes Campos Pavone" "FFLCH-FLH" "VERISSIMO, MARIA DE LA O RAMALLO" Limpar

Filtros

USP affiliated authors
- alonso, nivaldo (~2)
- bueno, maria rita dos santos e passos (~2)
- zatz, mayana (~2)
- ferreira, simone gomes (~1)
- kok, fernando (~1)
Date published
- 2015 (~2)
Subjects
- anormalidades do sistema nervoso (1)
- doenças metabólicas (1)
- erros inatos do metabolismo dos carboidratos (1)
- genética médica (1)
- lábio fissurado (1)

Artigo de periodico
Expanding the Molecular and Clinical Phenotype of SSR4-CDG (2015)
Ng, Bobby G.; Raymond, Kimiyo; Kircher, Martin; Buckingham, Kati J.; Wood, Tim; Shendure, Jay; Nickerson, Deborah A.; Bamshad, Michael J.; Wong, Jonathan T. S.; Monteiro, Fabiola Paoli; Graham, Brett H.; Jackson, Sheryl; Sparkes, Rebecca; Scheuerle, Angela E.; Cathey, Sara; Kok, Fernando; Gibson, James B.; Freeze, Hudson H.
Source: Human Mutation. Unidades: FM, IB
Subjects: ERROS INATOS DO METABOLISMO DOS CARBOIDRATOS, RECEPTORES, ANORMALIDADES DO SISTEMA NERVOSO, DOENÇAS METABÓLICAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
NG, Bobby G. et al. Expanding the Molecular and Clinical Phenotype of SSR4-CDG. Human Mutation, v. 36, n. 11, p. on-line, 2015Tradução . . Disponível em: http://onlinelibrary.wiley.com/doi/10.1002/humu.22856/epdf. Acesso em: 30 jun. 2024.
APA
Ng, B. G., Raymond, K., Kircher, M., Buckingham, K. J., Wood, T., Shendure, J., et al. (2015). Expanding the Molecular and Clinical Phenotype of SSR4-CDG. Human Mutation, 36( 11), on-line. doi:10.1002/humu.22856
NLM
Ng BG, Raymond K, Kircher M, Buckingham KJ, Wood T, Shendure J, Nickerson DA, Bamshad MJ, Wong JTS, Monteiro FP, Graham BH, Jackson S, Sparkes R, Scheuerle AE, Cathey S, Kok F, Gibson JB, Freeze HH. Expanding the Molecular and Clinical Phenotype of SSR4-CDG [Internet]. Human Mutation. 2015 ; 36( 11): on-line.[citado 2024 jun. 30 ] Available from: http://onlinelibrary.wiley.com/doi/10.1002/humu.22856/epdf
Vancouver
Ng BG, Raymond K, Kircher M, Buckingham KJ, Wood T, Shendure J, Nickerson DA, Bamshad MJ, Wong JTS, Monteiro FP, Graham BH, Jackson S, Sparkes R, Scheuerle AE, Cathey S, Kok F, Gibson JB, Freeze HH. Expanding the Molecular and Clinical Phenotype of SSR4-CDG [Internet]. Human Mutation. 2015 ; 36( 11): on-line.[citado 2024 jun. 30 ] Available from: http://onlinelibrary.wiley.com/doi/10.1002/humu.22856/epdf
Artigo de periodico
Rare variants in the epithelial cadherin gene underlying the genetic etiology of nonsyndromic cleft lip with or without cleft palat (2015)
Brito, Luciano Abreu; Yamamoto, Guilherme Lopes; Melo, Soraia; Malcher, Carolina; Ferreira, Simone Gomes; Figueiredo, Joana; Alvizi, Lucas; Kobayashi, Gerson Shigeru; Naslavsky, Michel ; Alonso, Nivaldo; Felix, Temis Maria; Zatz, Mayana ; Seruca, Raquel; Passos-Bueno, Maria Rita
Source: Human Mutation. Unidades: IB, FM
Subjects: GENÉTICA MÉDICA, VARIAÇÃO GENÉTICA, LÁBIO FISSURADO, NEOPLASIAS GÁSTRICAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
BRITO, Luciano Abreu et al. Rare variants in the epithelial cadherin gene underlying the genetic etiology of nonsyndromic cleft lip with or without cleft palat. Human Mutation, p. on-line, 2015Tradução . . Disponível em: https://doi.org/10.1002/humu.22827. Acesso em: 30 jun. 2024.
APA
Brito, L. A., Yamamoto, G. L., Melo, S., Malcher, C., Ferreira, S. G., Figueiredo, J., et al. (2015). Rare variants in the epithelial cadherin gene underlying the genetic etiology of nonsyndromic cleft lip with or without cleft palat. Human Mutation, on-line. doi:10.1002/humu.22827
NLM
Brito LA, Yamamoto GL, Melo S, Malcher C, Ferreira SG, Figueiredo J, Alvizi L, Kobayashi GS, Naslavsky M, Alonso N, Felix TM, Zatz M, Seruca R, Passos-Bueno MR. Rare variants in the epithelial cadherin gene underlying the genetic etiology of nonsyndromic cleft lip with or without cleft palat [Internet]. Human Mutation. 2015 ; on-line.[citado 2024 jun. 30 ] Available from: https://doi.org/10.1002/humu.22827
Vancouver
Brito LA, Yamamoto GL, Melo S, Malcher C, Ferreira SG, Figueiredo J, Alvizi L, Kobayashi GS, Naslavsky M, Alonso N, Felix TM, Zatz M, Seruca R, Passos-Bueno MR. Rare variants in the epithelial cadherin gene underlying the genetic etiology of nonsyndromic cleft lip with or without cleft palat [Internet]. Human Mutation. 2015 ; on-line.[citado 2024 jun. 30 ] Available from: https://doi.org/10.1002/humu.22827

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