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Artigo de periodico
Genetic etiology of non-syndromic hearing loss in Latin America (2022)
Lezirovitz, Karina ; Mingroni Netto, Regina Celia
Source: Human Genetics. Unidade: IB
Subjects: PERDA AUDITIVA, SURDEZ, MUTAÇÃO GENÉTICA
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LEZIROVITZ, Karina e MINGRONI NETTO, Regina Celia. Genetic etiology of non-syndromic hearing loss in Latin America. Human Genetics, v. 141, p. 539–581, 2022Tradução . . Disponível em: https://doi.org/10.1007/s00439-021-02354-4. Acesso em: 26 set. 2024.
APA
Lezirovitz, K., & Mingroni Netto, R. C. (2022). Genetic etiology of non-syndromic hearing loss in Latin America. Human Genetics, 141, 539–581. doi:10.1007/s00439-021-02354-4
NLM
Lezirovitz K, Mingroni Netto RC. Genetic etiology of non-syndromic hearing loss in Latin America [Internet]. Human Genetics. 2022 ; 141 539–581.[citado 2024 set. 26 ] Available from: https://doi.org/10.1007/s00439-021-02354-4
Vancouver
Lezirovitz K, Mingroni Netto RC. Genetic etiology of non-syndromic hearing loss in Latin America [Internet]. Human Genetics. 2022 ; 141 539–581.[citado 2024 set. 26 ] Available from: https://doi.org/10.1007/s00439-021-02354-4
Artigo de periodico
Correction to: genetic etiology of non-syndromic hearing loss in Latin America (2022)
Lezirovitz, Karina ; Mingroni Netto, Regina Celia
Source: Human Genetics. Unidade: IB
Subjects: PERDA AUDITIVA, SURDEZ, MUTAÇÃO GENÉTICA
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LEZIROVITZ, Karina e MINGRONI NETTO, Regina Celia. Correction to: genetic etiology of non-syndromic hearing loss in Latin America. Human Genetics, v. 141, p. 997, 2022Tradução . . Disponível em: https://doi.org/10.1007/s00439-021-02354-4. Acesso em: 26 set. 2024.
APA
Lezirovitz, K., & Mingroni Netto, R. C. (2022). Correction to: genetic etiology of non-syndromic hearing loss in Latin America. Human Genetics, 141, 997. doi:10.1007/s00439-021-02354-4
NLM
Lezirovitz K, Mingroni Netto RC. Correction to: genetic etiology of non-syndromic hearing loss in Latin America [Internet]. Human Genetics. 2022 ; 141 997.[citado 2024 set. 26 ] Available from: https://doi.org/10.1007/s00439-021-02354-4
Vancouver
Lezirovitz K, Mingroni Netto RC. Correction to: genetic etiology of non-syndromic hearing loss in Latin America [Internet]. Human Genetics. 2022 ; 141 997.[citado 2024 set. 26 ] Available from: https://doi.org/10.1007/s00439-021-02354-4
Artigo de periodico
Further delineation of nonhomologous-based recombination and evidence for subtelomeric segmental duplications in 1p36 rearrangements (2009)
D'Angelo, Carla S.; Gajecka, Marzena; Kim, Chong A.; Gentles, Andrew J.; Glotzbach, Caron D.; Shaffer, Lisa G.; Koiffmann, Celia Priszkulnik
Source: Human Genetics. Unidade: IB
Assunto: ANORMALIDADES CROMOSSÔMICAS
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D'ANGELO, Carla S. et al. Further delineation of nonhomologous-based recombination and evidence for subtelomeric segmental duplications in 1p36 rearrangements. Human Genetics, v. 125, n. 6, p. 551-563, 2009Tradução . . Disponível em: https://doi.org/10.1007/s00439-009-0650-9. Acesso em: 26 set. 2024.
APA
D'Angelo, C. S., Gajecka, M., Kim, C. A., Gentles, A. J., Glotzbach, C. D., Shaffer, L. G., & Koiffmann, C. P. (2009). Further delineation of nonhomologous-based recombination and evidence for subtelomeric segmental duplications in 1p36 rearrangements. Human Genetics, 125( 6), 551-563. doi:10.1007/s00439-009-0650-9
NLM
D'Angelo CS, Gajecka M, Kim CA, Gentles AJ, Glotzbach CD, Shaffer LG, Koiffmann CP. Further delineation of nonhomologous-based recombination and evidence for subtelomeric segmental duplications in 1p36 rearrangements [Internet]. Human Genetics. 2009 ; 125( 6): 551-563.[citado 2024 set. 26 ] Available from: https://doi.org/10.1007/s00439-009-0650-9
Vancouver
D'Angelo CS, Gajecka M, Kim CA, Gentles AJ, Glotzbach CD, Shaffer LG, Koiffmann CP. Further delineation of nonhomologous-based recombination and evidence for subtelomeric segmental duplications in 1p36 rearrangements [Internet]. Human Genetics. 2009 ; 125( 6): 551-563.[citado 2024 set. 26 ] Available from: https://doi.org/10.1007/s00439-009-0650-9
Artigo de periodico
A novel association of a polymorphism in the first intron of adiponectin gene with type 2 diabetes, obesity and hypoadiponectinemia in Asian Indians (2008)
Lezirovitz, Karina; Maestrelli, Sylvia Regina Pedrosa; Cotrim, Nelson Henderson; Otto, Paulo A ; Pearson, Peter Lees; Mingroni Netto, Regina Celia
Source: Human Genetics. Unidade: IB
Subjects: DOENÇAS HEREDITÁRIAS, MUTAÇÃO GENÉTICA
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ABNT
LEZIROVITZ, Karina et al. A novel association of a polymorphism in the first intron of adiponectin gene with type 2 diabetes, obesity and hypoadiponectinemia in Asian Indians. Human Genetics, v. 123, n. 6, p. 625-631, 2008Tradução . . Acesso em: 26 set. 2024.
APA
Lezirovitz, K., Maestrelli, S. R. P., Cotrim, N. H., Otto, P. A., Pearson, P. L., & Mingroni Netto, R. C. (2008). A novel association of a polymorphism in the first intron of adiponectin gene with type 2 diabetes, obesity and hypoadiponectinemia in Asian Indians. Human Genetics, 123( 6), 625-631.
NLM
Lezirovitz K, Maestrelli SRP, Cotrim NH, Otto PA, Pearson PL, Mingroni Netto RC. A novel association of a polymorphism in the first intron of adiponectin gene with type 2 diabetes, obesity and hypoadiponectinemia in Asian Indians. Human Genetics. 2008 ; 123( 6): 625-631.[citado 2024 set. 26 ]
Vancouver
Lezirovitz K, Maestrelli SRP, Cotrim NH, Otto PA, Pearson PL, Mingroni Netto RC. A novel association of a polymorphism in the first intron of adiponectin gene with type 2 diabetes, obesity and hypoadiponectinemia in Asian Indians. Human Genetics. 2008 ; 123( 6): 625-631.[citado 2024 set. 26 ]
Artigo de periodico
A novel locus for split-hand/foot malformation associated with tibial hemimelia (SHFLD syndrome) maps to chromosome region 17p13.1-17p13.3 (2008)
Lezirovitz, Karina; Maestrelli, Sylvia Regina Pedrosa; Cotrim, Nelson Henderson; Otto, Paulo A ; Pearson, Peter Lees; Mingroni Netto, Regina Celia
Source: Human Genetics. Unidade: IB
Subjects: DOENÇAS GENÉTICAS, MALFORMAÇÕES
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LEZIROVITZ, Karina et al. A novel locus for split-hand/foot malformation associated with tibial hemimelia (SHFLD syndrome) maps to chromosome region 17p13.1-17p13.3. Human Genetics, v. 123, n. 6, p. 625-631, 2008Tradução . . Disponível em: https://doi.org/10.1007/s00439-008-0515-7. Acesso em: 26 set. 2024.
APA
Lezirovitz, K., Maestrelli, S. R. P., Cotrim, N. H., Otto, P. A., Pearson, P. L., & Mingroni Netto, R. C. (2008). A novel locus for split-hand/foot malformation associated with tibial hemimelia (SHFLD syndrome) maps to chromosome region 17p13.1-17p13.3. Human Genetics, 123( 6), 625-631. doi:10.1007/s00439-008-0515-7
NLM
Lezirovitz K, Maestrelli SRP, Cotrim NH, Otto PA, Pearson PL, Mingroni Netto RC. A novel locus for split-hand/foot malformation associated with tibial hemimelia (SHFLD syndrome) maps to chromosome region 17p13.1-17p13.3 [Internet]. Human Genetics. 2008 ; 123( 6): 625-631.[citado 2024 set. 26 ] Available from: https://doi.org/10.1007/s00439-008-0515-7
Vancouver
Lezirovitz K, Maestrelli SRP, Cotrim NH, Otto PA, Pearson PL, Mingroni Netto RC. A novel locus for split-hand/foot malformation associated with tibial hemimelia (SHFLD syndrome) maps to chromosome region 17p13.1-17p13.3 [Internet]. Human Genetics. 2008 ; 123( 6): 625-631.[citado 2024 set. 26 ] Available from: https://doi.org/10.1007/s00439-008-0515-7
Artigo de periodico
Equal proportions of affected cells in muscle and blood of a mosaic carrier of facioscapulohumeral muscular dystrophy (2006)
Tonini, Maria Manuela O; Lemmers, Richard J.L.F; Pavanello, Rita C M; Cerqueira, Antonia M.P; Frants, Rune R; Maarel, Silvere M. van der ; Zatz, Mayana
Source: Human Genetics. Unidade: IB
Subjects: DISTROFIA MUSCULAR, BIOLOGIA CELULAR, MÚSCULOS, SANGUE, DNA
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TONINI, Maria Manuela O et al. Equal proportions of affected cells in muscle and blood of a mosaic carrier of facioscapulohumeral muscular dystrophy. Human Genetics, v. 119, p. 23-28, 2006Tradução . . Disponível em: https://doi.org/10.1007/s00439-005-0100-2. Acesso em: 26 set. 2024.
APA
Tonini, M. M. O., Lemmers, R. J. L. F., Pavanello, R. C. M., Cerqueira, A. M. P., Frants, R. R., Maarel, S. M. van der, & Zatz, M. (2006). Equal proportions of affected cells in muscle and blood of a mosaic carrier of facioscapulohumeral muscular dystrophy. Human Genetics, 119, 23-28. doi:10.1007/s00439-005-0100-2
NLM
Tonini MMO, Lemmers RJLF, Pavanello RCM, Cerqueira AMP, Frants RR, Maarel SM van der, Zatz M. Equal proportions of affected cells in muscle and blood of a mosaic carrier of facioscapulohumeral muscular dystrophy [Internet]. Human Genetics. 2006 ; 119 23-28.[citado 2024 set. 26 ] Available from: https://doi.org/10.1007/s00439-005-0100-2
Vancouver
Tonini MMO, Lemmers RJLF, Pavanello RCM, Cerqueira AMP, Frants RR, Maarel SM van der, Zatz M. Equal proportions of affected cells in muscle and blood of a mosaic carrier of facioscapulohumeral muscular dystrophy [Internet]. Human Genetics. 2006 ; 119 23-28.[citado 2024 set. 26 ] Available from: https://doi.org/10.1007/s00439-005-0100-2
Artigo de periodico
X chromosome-inactivation patterns in patients with Rett syndrome (1998)
Krepischi, Ana Cristina Victorino ; Kok, Fernando; Otto, Priscila Guimarães
Source: Human Genetics. Unidade: IB
Assunto: BIOLOGIA MOLECULAR
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ABNT
KREPISCHI, Ana Cristina Victorino e KOK, Fernando e OTTO, Priscila Guimarães. X chromosome-inactivation patterns in patients with Rett syndrome. Human Genetics, v. 102, p. 319-321, 1998Tradução . . Disponível em: https://doi.org/10.1007/s004390050698. Acesso em: 26 set. 2024.
APA
Krepischi, A. C. V., Kok, F., & Otto, P. G. (1998). X chromosome-inactivation patterns in patients with Rett syndrome. Human Genetics, 102, 319-321. doi:10.1007/s004390050698
NLM
Krepischi ACV, Kok F, Otto PG. X chromosome-inactivation patterns in patients with Rett syndrome [Internet]. Human Genetics. 1998 ; 102 319-321.[citado 2024 set. 26 ] Available from: https://doi.org/10.1007/s004390050698
Vancouver
Krepischi ACV, Kok F, Otto PG. X chromosome-inactivation patterns in patients with Rett syndrome [Internet]. Human Genetics. 1998 ; 102 319-321.[citado 2024 set. 26 ] Available from: https://doi.org/10.1007/s004390050698
Artigo de periodico
RB1 deletion in gonadoblastoma in an XY female (1997)
Antonini, S; Barbosa, A S; Rosenberg, Carla ; Barbosa, A C C; Moreira-Filho, Carlos Alberto; Vianna-Morgante, Angela M
Source: Human Genetics. Unidades: IB, ICB
Assunto: IMUNOLOGIA
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ANTONINI, S et al. RB1 deletion in gonadoblastoma in an XY female. Human Genetics, v. 101, p. 181-185, 1997Tradução . . Disponível em: https://doi.org/10.1007/s004390050610. Acesso em: 26 set. 2024.
APA
Antonini, S., Barbosa, A. S., Rosenberg, C., Barbosa, A. C. C., Moreira-Filho, C. A., & Vianna-Morgante, A. M. (1997). RB1 deletion in gonadoblastoma in an XY female. Human Genetics, 101, 181-185. doi:10.1007/s004390050610
NLM
Antonini S, Barbosa AS, Rosenberg C, Barbosa ACC, Moreira-Filho CA, Vianna-Morgante AM. RB1 deletion in gonadoblastoma in an XY female [Internet]. Human Genetics. 1997 ; 101 181-185.[citado 2024 set. 26 ] Available from: https://doi.org/10.1007/s004390050610
Vancouver
Antonini S, Barbosa AS, Rosenberg C, Barbosa ACC, Moreira-Filho CA, Vianna-Morgante AM. RB1 deletion in gonadoblastoma in an XY female [Internet]. Human Genetics. 1997 ; 101 181-185.[citado 2024 set. 26 ] Available from: https://doi.org/10.1007/s004390050610
Artigo de periodico
Pcr-based test suitable for screening for fragile x syndrome among mentally retarded males (1996)
Haddad, Luciana Amaral ; Mingroni Netto, Regina Celia ; Vianna-Morgante, Angela M ; Pena, S D J
Source: Human Genetics. Unidade: IB
Assunto: GENÉTICA MÉDICA
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HADDAD, Luciana Amaral et al. Pcr-based test suitable for screening for fragile x syndrome among mentally retarded males. Human Genetics, v. 97, p. 808-12, 1996Tradução . . Disponível em: https://doi.org/10.1007/s004390050141. Acesso em: 26 set. 2024.
APA
Haddad, L. A., Mingroni Netto, R. C., Vianna-Morgante, A. M., & Pena, S. D. J. (1996). Pcr-based test suitable for screening for fragile x syndrome among mentally retarded males. Human Genetics, 97, 808-12. doi:10.1007/s004390050141
NLM
Haddad LA, Mingroni Netto RC, Vianna-Morgante AM, Pena SDJ. Pcr-based test suitable for screening for fragile x syndrome among mentally retarded males [Internet]. Human Genetics. 1996 ;97 808-12.[citado 2024 set. 26 ] Available from: https://doi.org/10.1007/s004390050141
Vancouver
Haddad LA, Mingroni Netto RC, Vianna-Morgante AM, Pena SDJ. Pcr-based test suitable for screening for fragile x syndrome among mentally retarded males [Internet]. Human Genetics. 1996 ;97 808-12.[citado 2024 set. 26 ] Available from: https://doi.org/10.1007/s004390050141
Artigo de periodico
Is shwachman syndrome (mckusick 26040) a chromosome breakage syndrome? (1991)
Koiffmann, Celia Priszkulnik ; Gonzalez, Claudette Hajaj; Souza, D. H.; Romani, E G; Kim, C A; Wajntal, Anita
Source: Human Genetics. Unidades: IB, FM
Assunto: GENÉTICA MÉDICA
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KOIFFMANN, Celia Priszkulnik et al. Is shwachman syndrome (mckusick 26040) a chromosome breakage syndrome?. Human Genetics, v. 87, n. 1 , p. 106-7, 1991Tradução . . Disponível em: https://doi.org/10.1007/bf01213107. Acesso em: 26 set. 2024.
APA
Koiffmann, C. P., Gonzalez, C. H., Souza, D. H., Romani, E. G., Kim, C. A., & Wajntal, A. (1991). Is shwachman syndrome (mckusick 26040) a chromosome breakage syndrome? Human Genetics, 87( 1 ), 106-7. doi:10.1007/bf01213107
NLM
Koiffmann CP, Gonzalez CH, Souza DH, Romani EG, Kim CA, Wajntal A. Is shwachman syndrome (mckusick 26040) a chromosome breakage syndrome? [Internet]. Human Genetics. 1991 ;87( 1 ): 106-7.[citado 2024 set. 26 ] Available from: https://doi.org/10.1007/bf01213107
Vancouver
Koiffmann CP, Gonzalez CH, Souza DH, Romani EG, Kim CA, Wajntal A. Is shwachman syndrome (mckusick 26040) a chromosome breakage syndrome? [Internet]. Human Genetics. 1991 ;87( 1 ): 106-7.[citado 2024 set. 26 ] Available from: https://doi.org/10.1007/bf01213107
Artigo de periodico
In search of a genetic basis for the rett syndrome (1990)
Martinho, P S; Otto, Priscila Guimarães; Kok, F; Diament, Aron Judka; Marques Dias, M J; Gonzalez, Claudette Hajaj
Source: Human Genetics. Unidades: FM, IB
Subjects: GENÉTICA MÉDICA, NEUROLOGIA
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MARTINHO, P S et al. In search of a genetic basis for the rett syndrome. Human Genetics, v. 86, p. 131-4, 1990Tradução . . Disponível em: https://doi.org/10.1007/bf00197693. Acesso em: 26 set. 2024.
APA
Martinho, P. S., Otto, P. G., Kok, F., Diament, A. J., Marques Dias, M. J., & Gonzalez, C. H. (1990). In search of a genetic basis for the rett syndrome. Human Genetics, 86, 131-4. doi:10.1007/bf00197693
NLM
Martinho PS, Otto PG, Kok F, Diament AJ, Marques Dias MJ, Gonzalez CH. In search of a genetic basis for the rett syndrome [Internet]. Human Genetics. 1990 ;86 131-4.[citado 2024 set. 26 ] Available from: https://doi.org/10.1007/bf00197693
Vancouver
Martinho PS, Otto PG, Kok F, Diament AJ, Marques Dias MJ, Gonzalez CH. In search of a genetic basis for the rett syndrome [Internet]. Human Genetics. 1990 ;86 131-4.[citado 2024 set. 26 ] Available from: https://doi.org/10.1007/bf00197693
Artigo de periodico
What cause the abnormal phenotype in a 49, xxxxy male? (1987)
Sarto, G E; Otto, Priscila Guimarães; Kuhn, E M; Therman, E
Source: Human Genetics. Unidade: IB
Assunto: GENÉTICA MÉDICA
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ABNT
SARTO, G E et al. What cause the abnormal phenotype in a 49, xxxxy male?. Human Genetics, v. 76, p. 1-4, 1987Tradução . . Acesso em: 26 set. 2024.
APA
Sarto, G. E., Otto, P. G., Kuhn, E. M., & Therman, E. (1987). What cause the abnormal phenotype in a 49, xxxxy male? Human Genetics, 76, 1-4.
NLM
Sarto GE, Otto PG, Kuhn EM, Therman E. What cause the abnormal phenotype in a 49, xxxxy male? Human Genetics. 1987 ;76 1-4.[citado 2024 set. 26 ]
Vancouver
Sarto GE, Otto PG, Kuhn EM, Therman E. What cause the abnormal phenotype in a 49, xxxxy male? Human Genetics. 1987 ;76 1-4.[citado 2024 set. 26 ]
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
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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: 26 set. 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 set. 26 ] 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 set. 26 ] Available from: https://doi.org/10.1007/bf00281686
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
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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: 26 set. 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 set. 26 ] 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 set. 26 ] Available from: https://doi.org/10.1007/bf00282013
Artigo de periodico
Paternal or maternal origin of human i(Xq) isochromosomes (1981)
Otto, Paulo A ; Otto, Priscila Guimarães
Source: Human Genetics. Unidade: IB
Assunto: PATERNIDADE (TESTES)
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ABNT
OTTO, Paulo A e OTTO, Priscila Guimarães. Paternal or maternal origin of human i(Xq) isochromosomes. Human Genetics, v. 59, p. 308-309, 1981Tradução . . Disponível em: https://doi.org/10.1007/bf00295462. Acesso em: 26 set. 2024.
APA
Otto, P. A., & Otto, P. G. (1981). Paternal or maternal origin of human i(Xq) isochromosomes. Human Genetics, 59, 308-309. doi:10.1007/bf00295462
NLM
Otto PA, Otto PG. Paternal or maternal origin of human i(Xq) isochromosomes [Internet]. Human Genetics. 1981 ; 59 308-309.[citado 2024 set. 26 ] Available from: https://doi.org/10.1007/bf00295462
Vancouver
Otto PA, Otto PG. Paternal or maternal origin of human i(Xq) isochromosomes [Internet]. Human Genetics. 1981 ; 59 308-309.[citado 2024 set. 26 ] Available from: https://doi.org/10.1007/bf00295462
Artigo de periodico
H-Y antigen expression in a case of XX true hermaphroditism (1980)
Moreira Filho, C. A.; Otto, Priscila Guimarães; Mustacchi, Zan; Frota-Pessoa, Oswaldo; Otto, Paulo A
Source: Human Genetics. Unidade: IB
Assunto: HERMAFRODITISMO
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ABNT
MOREIRA FILHO, C. A. et al. H-Y antigen expression in a case of XX true hermaphroditism. Human Genetics, v. 55, p. 309-314, 1980Tradução . . Disponível em: https://doi.org/10.1007/bf00290209. Acesso em: 26 set. 2024.
APA
Moreira Filho, C. A., Otto, P. G., Mustacchi, Z., Frota-Pessoa, O., & Otto, P. A. (1980). H-Y antigen expression in a case of XX true hermaphroditism. Human Genetics, 55, 309-314. doi:10.1007/bf00290209
NLM
Moreira Filho CA, Otto PG, Mustacchi Z, Frota-Pessoa O, Otto PA. H-Y antigen expression in a case of XX true hermaphroditism [Internet]. Human Genetics. 1980 ; 55 309-314.[citado 2024 set. 26 ] Available from: https://doi.org/10.1007/bf00290209
Vancouver
Moreira Filho CA, Otto PG, Mustacchi Z, Frota-Pessoa O, Otto PA. H-Y antigen expression in a case of XX true hermaphroditism [Internet]. Human Genetics. 1980 ; 55 309-314.[citado 2024 set. 26 ] Available from: https://doi.org/10.1007/bf00290209
Artigo de periodico
H-Y antigen in Swyer syndrome and the genetics of XY gonadal dysgenesis (1979)
Moreira-Filho, Carlos Alberto; Toledo, Sérgio Pereira de Alemida; Bagnolli, Vicente Renato; Frota-Pessoa, Oswaldo; Bisi, Hélio; Wajntal, Anita
Source: Human Genetics. Unidades: ICB, FM, IB
Assunto: CROMOSSOMOS HUMANOS (ANORMALIDADES)
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ABNT
MOREIRA-FILHO, Carlos Alberto et al. H-Y antigen in Swyer syndrome and the genetics of XY gonadal dysgenesis. Human Genetics, v. 53, p. 51-56, 1979Tradução . . Disponível em: https://doi.org/10.1007/bf00289451. Acesso em: 26 set. 2024.
APA
Moreira-Filho, C. A., Toledo, S. P. de A., Bagnolli, V. R., Frota-Pessoa, O., Bisi, H., & Wajntal, A. (1979). H-Y antigen in Swyer syndrome and the genetics of XY gonadal dysgenesis. Human Genetics, 53, 51-56. doi:10.1007/bf00289451
NLM
Moreira-Filho CA, Toledo SP de A, Bagnolli VR, Frota-Pessoa O, Bisi H, Wajntal A. H-Y antigen in Swyer syndrome and the genetics of XY gonadal dysgenesis [Internet]. Human Genetics. 1979 ; 53 51-56.[citado 2024 set. 26 ] Available from: https://doi.org/10.1007/bf00289451
Vancouver
Moreira-Filho CA, Toledo SP de A, Bagnolli VR, Frota-Pessoa O, Bisi H, Wajntal A. H-Y antigen in Swyer syndrome and the genetics of XY gonadal dysgenesis [Internet]. Human Genetics. 1979 ; 53 51-56.[citado 2024 set. 26 ] Available from: https://doi.org/10.1007/bf00289451
Artigo de periodico
Partial monosomy 13 and 21 due to a familial 13/21 translocation (1978)
Otto, Priscila Guimarães; Toledo, Sérgio; Richieri-Costa, Antonio; Otto, Paulo A ; Vianna-Morgante, Angela M ; Kasahara, Sanae
Source: Human Genetics. Unidade: IB
Assunto: ANORMALIDADES CROMOSSÔMICAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
OTTO, Priscila Guimarães et al. Partial monosomy 13 and 21 due to a familial 13/21 translocation. Human Genetics, v. 41, p. 243-250, 1978Tradução . . Disponível em: https://doi.org/10.1007/bf00284757. Acesso em: 26 set. 2024.
APA
Otto, P. G., Toledo, S., Richieri-Costa, A., Otto, P. A., Vianna-Morgante, A. M., & Kasahara, S. (1978). Partial monosomy 13 and 21 due to a familial 13/21 translocation. Human Genetics, 41, 243-250. doi:10.1007/bf00284757
NLM
Otto PG, Toledo S, Richieri-Costa A, Otto PA, Vianna-Morgante AM, Kasahara S. Partial monosomy 13 and 21 due to a familial 13/21 translocation [Internet]. Human Genetics. 1978 ; 41 243-250.[citado 2024 set. 26 ] Available from: https://doi.org/10.1007/bf00284757
Vancouver
Otto PG, Toledo S, Richieri-Costa A, Otto PA, Vianna-Morgante AM, Kasahara S. Partial monosomy 13 and 21 due to a familial 13/21 translocation [Internet]. Human Genetics. 1978 ; 41 243-250.[citado 2024 set. 26 ] Available from: https://doi.org/10.1007/bf00284757

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