ReP USP - Resultado da busca

Artigo de periodico
Pathogenic mutations in GLI2 cause a specific phenotype that is distinct from holoprosencephaly (2014)
Bear, Kelly A.; Solomon, Benjamin D.; Antonini, Sonir; Arnhold, Ivo J. P.; França, Marcela M.; Gerkes, Erica H.; Grange, Dorothy K.; Hadley, Donald W.; Jääskeläinen, Jarmo; Paulo, Sabrina S.; Rump, Patrick; Stratakis, Constantine A.; Thompson, Elizabeth M.; Willis, Mary; Winder, Thomas L.; Jorge, Alexander A. L.; Roessler, Erich; Muenke, Maximilian
Source: Journal of Medical Genetics. Unidade: FM
Subjects: FENÓTIPOS, MUTAÇÃO GENÉTICA, NEUROANATOMIA (ANOMALAIS), HOLOPROSENCEFALIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
BEAR, Kelly A. et al. Pathogenic mutations in GLI2 cause a specific phenotype that is distinct from holoprosencephaly. Journal of Medical Genetics, v. 51, n. 6, p. 413-418, 2014Tradução . . Disponível em: https://doi.org/10.1136/jmedgenet-2013-102249. Acesso em: 12 maio 2024.
APA
Bear, K. A., Solomon, B. D., Antonini, S., Arnhold, I. J. P., França, M. M., Gerkes, E. H., et al. (2014). Pathogenic mutations in GLI2 cause a specific phenotype that is distinct from holoprosencephaly. Journal of Medical Genetics, 51( 6), 413-418. doi:10.1136/jmedgenet-2013-102249
NLM
Bear KA, Solomon BD, Antonini S, Arnhold IJP, França MM, Gerkes EH, Grange DK, Hadley DW, Jääskeläinen J, Paulo SS, Rump P, Stratakis CA, Thompson EM, Willis M, Winder TL, Jorge AAL, Roessler E, Muenke M. Pathogenic mutations in GLI2 cause a specific phenotype that is distinct from holoprosencephaly [Internet]. Journal of Medical Genetics. 2014 ; 51( 6): 413-418.[citado 2024 maio 12 ] Available from: https://doi.org/10.1136/jmedgenet-2013-102249
Vancouver
Bear KA, Solomon BD, Antonini S, Arnhold IJP, França MM, Gerkes EH, Grange DK, Hadley DW, Jääskeläinen J, Paulo SS, Rump P, Stratakis CA, Thompson EM, Willis M, Winder TL, Jorge AAL, Roessler E, Muenke M. Pathogenic mutations in GLI2 cause a specific phenotype that is distinct from holoprosencephaly [Internet]. Journal of Medical Genetics. 2014 ; 51( 6): 413-418.[citado 2024 maio 12 ] Available from: https://doi.org/10.1136/jmedgenet-2013-102249
Artigo de periodico
Comparison of mutation findings in ZIC2 between microform and classical holoprosencephaly in a Brazilian cohort (2012)
Ribeiro, Lucilene Arilho; Roessler, Erich; Hu, Ping; Pineda-Alvarez, Daniel E.; Zhou, Nan; Jones, MaryPat; Chandrasekharappa, Settara; Richieri-Costa, Antonio ; Muenke, Maximilian
Source: Birth Defects Research. Part A, Clinical and Molecular Teratology.. Unidade: HRAC
Subjects: HOLOPROSENCEFALIA, POLIMORFISMO, MUTAÇÃO GENÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
RIBEIRO, Lucilene Arilho et al. Comparison of mutation findings in ZIC2 between microform and classical holoprosencephaly in a Brazilian cohort. Birth Defects Research. Part A, Clinical and Molecular Teratology., v. No 2012, n. 11, p. 912-917, 2012Tradução . . Disponível em: https://doi.org/10.1002/bdra.23047. Acesso em: 12 maio 2024.
APA
Ribeiro, L. A., Roessler, E., Hu, P., Pineda-Alvarez, D. E., Zhou, N., Jones, M. P., et al. (2012). Comparison of mutation findings in ZIC2 between microform and classical holoprosencephaly in a Brazilian cohort. Birth Defects Research. Part A, Clinical and Molecular Teratology., No 2012( 11), 912-917. doi:10.1002/bdra.23047
NLM
Ribeiro LA, Roessler E, Hu P, Pineda-Alvarez DE, Zhou N, Jones MP, Chandrasekharappa S, Richieri-Costa A, Muenke M. Comparison of mutation findings in ZIC2 between microform and classical holoprosencephaly in a Brazilian cohort [Internet]. Birth Defects Research. Part A, Clinical and Molecular Teratology. 2012 ; No 2012( 11): 912-917.[citado 2024 maio 12 ] Available from: https://doi.org/10.1002/bdra.23047
Vancouver
Ribeiro LA, Roessler E, Hu P, Pineda-Alvarez DE, Zhou N, Jones MP, Chandrasekharappa S, Richieri-Costa A, Muenke M. Comparison of mutation findings in ZIC2 between microform and classical holoprosencephaly in a Brazilian cohort [Internet]. Birth Defects Research. Part A, Clinical and Molecular Teratology. 2012 ; No 2012( 11): 912-917.[citado 2024 maio 12 ] Available from: https://doi.org/10.1002/bdra.23047
Artigo de periodico
Mutations in the homeodomain of the human SIX3 gene cause holoprosencephaly (1999)
Wallis, Deeann E.; Roessler, Erich; Hehr, Ute; Nanni, Luisa; Wiltshire, Tim; Richieri-Costa, Antonio; Gillessen-Kaesbach, Gabriele; Zackai, Elaine H.; Rommens, Johanna; Muenke, Maximilian
Source: Nature Genetics. Unidade: HRAC
Assunto: GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
WALLIS, Deeann E. et al. Mutations in the homeodomain of the human SIX3 gene cause holoprosencephaly. Nature Genetics, v. 22, n. 2, p. 196-198, 1999Tradução . . Disponível em: https://doi.org/10.1038/9718. Acesso em: 12 maio 2024.
APA
Wallis, D. E., Roessler, E., Hehr, U., Nanni, L., Wiltshire, T., Richieri-Costa, A., et al. (1999). Mutations in the homeodomain of the human SIX3 gene cause holoprosencephaly. Nature Genetics, 22( 2), 196-198. doi:10.1038/9718
NLM
Wallis DE, Roessler E, Hehr U, Nanni L, Wiltshire T, Richieri-Costa A, Gillessen-Kaesbach G, Zackai EH, Rommens J, Muenke M. Mutations in the homeodomain of the human SIX3 gene cause holoprosencephaly [Internet]. Nature Genetics. 1999 ; 22( 2): 196-198.[citado 2024 maio 12 ] Available from: https://doi.org/10.1038/9718
Vancouver
Wallis DE, Roessler E, Hehr U, Nanni L, Wiltshire T, Richieri-Costa A, Gillessen-Kaesbach G, Zackai EH, Rommens J, Muenke M. Mutations in the homeodomain of the human SIX3 gene cause holoprosencephaly [Internet]. Nature Genetics. 1999 ; 22( 2): 196-198.[citado 2024 maio 12 ] Available from: https://doi.org/10.1038/9718

USP Schools

ReP

Filtros

Authors

Subjects

Indexado em