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Artigo de periodico
H-Y antigen expression in a case of mixed gonadal dysgenesis (1981)
Moreira Filho, C. A.; Amaral, Antonia Tavares do ; Otto, Paulo A ; Vianna-Morgante, Angela M ; Otto, Priscila Guimarães; Elejalde, B. R.
Source: Human Genetics. Unidade: IB
Assunto: GONADOTROFINAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MOREIRA FILHO, C. A. et al. H-Y antigen expression in a case of mixed gonadal dysgenesis. Human Genetics, v. 57, p. 366-370, 1981Tradução . . Disponível em: https://doi.org/10.1007/bf00281686. Acesso em: 22 ago. 2024.
APA
Moreira Filho, C. A., Amaral, A. T. do, Otto, P. A., Vianna-Morgante, A. M., Otto, P. G., & Elejalde, B. R. (1981). H-Y antigen expression in a case of mixed gonadal dysgenesis. Human Genetics, 57, 366-370. doi:10.1007/bf00281686
NLM
Moreira Filho CA, Amaral AT do, Otto PA, Vianna-Morgante AM, Otto PG, Elejalde BR. H-Y antigen expression in a case of mixed gonadal dysgenesis [Internet]. Human Genetics. 1981 ; 57 366-370.[citado 2024 ago. 22 ] Available from: https://doi.org/10.1007/bf00281686
Vancouver
Moreira Filho CA, Amaral AT do, Otto PA, Vianna-Morgante AM, Otto PG, Elejalde BR. H-Y antigen expression in a case of mixed gonadal dysgenesis [Internet]. Human Genetics. 1981 ; 57 366-370.[citado 2024 ago. 22 ] Available from: https://doi.org/10.1007/bf00281686
Artigo de periodico
Traslocation (X;6) in a female with Duchenne muscular dystrophy: implications for the localisation of the DMD locus (1981)
Zatz, Mayana ; Vianna-Morgante, Angela M ; Campos, Patrícia; Diament, Aron Judka
Source: Journal of Medical Genetics. Unidades: IB, FM
Subjects: DOENÇAS GENÉTICAS, DISTROFIA MUSCULAR
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ZATZ, Mayana et al. Traslocation (X;6) in a female with Duchenne muscular dystrophy: implications for the localisation of the DMD locus. Journal of Medical Genetics, v. 18, p. 442-447, 1981Tradução . . Disponível em: https://doi.org/10.1136/jmg.18.6.442. Acesso em: 22 ago. 2024.
APA
Zatz, M., Vianna-Morgante, A. M., Campos, P., & Diament, A. J. (1981). Traslocation (X;6) in a female with Duchenne muscular dystrophy: implications for the localisation of the DMD locus. Journal of Medical Genetics, 18, 442-447. doi:10.1136/jmg.18.6.442
NLM
Zatz M, Vianna-Morgante AM, Campos P, Diament AJ. Traslocation (X;6) in a female with Duchenne muscular dystrophy: implications for the localisation of the DMD locus [Internet]. Journal of Medical Genetics. 1981 ; 18 442-447.[citado 2024 ago. 22 ] Available from: https://doi.org/10.1136/jmg.18.6.442
Vancouver
Zatz M, Vianna-Morgante AM, Campos P, Diament AJ. Traslocation (X;6) in a female with Duchenne muscular dystrophy: implications for the localisation of the DMD locus [Internet]. Journal of Medical Genetics. 1981 ; 18 442-447.[citado 2024 ago. 22 ] Available from: https://doi.org/10.1136/jmg.18.6.442
Artigo de periodico
The turner phenotype and the different types of human X isochromosome (1981)
Otto, Priscila Guimarães; Vianna-Morgante, Angela M ; Otto, Paulo A ; Wajntal, Anita
Source: Human Genetics. Unidade: IB
Subjects: DOENÇAS GENÉTICAS, CARIOTIPAGEM
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
OTTO, Priscila Guimarães et al. The turner phenotype and the different types of human X isochromosome. Human Genetics, v. 57, p. 159-164, 1981Tradução . . Disponível em: https://doi.org/10.1007/bf00282013. Acesso em: 22 ago. 2024.
APA
Otto, P. G., Vianna-Morgante, A. M., Otto, P. A., & Wajntal, A. (1981). The turner phenotype and the different types of human X isochromosome. Human Genetics, 57, 159-164. doi:10.1007/bf00282013
NLM
Otto PG, Vianna-Morgante AM, Otto PA, Wajntal A. The turner phenotype and the different types of human X isochromosome [Internet]. Human Genetics. 1981 ; 57 159-164.[citado 2024 ago. 22 ] Available from: https://doi.org/10.1007/bf00282013
Vancouver
Otto PG, Vianna-Morgante AM, Otto PA, Wajntal A. The turner phenotype and the different types of human X isochromosome [Internet]. Human Genetics. 1981 ; 57 159-164.[citado 2024 ago. 22 ] Available from: https://doi.org/10.1007/bf00282013

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