ReP USP - Resultado da busca

Artigo de periodico
Direct and indirect impact of SARS-CoV-2 on the brain (2023)
Peron, Jean Pierre Schatzmann
Source: Human Genetics. Unidade: ICB
Subjects: IMUNOLOGIA, COVID-19, SISTEMA NERVOSO CENTRAL
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
PERON, Jean Pierre Schatzmann. Direct and indirect impact of SARS-CoV-2 on the brain. Human Genetics, p. 1-10, 2023Tradução . . Disponível em: https://doi.org/10.1007/s00439-023-02549-x. Acesso em: 28 set. 2024.
APA
Peron, J. P. S. (2023). Direct and indirect impact of SARS-CoV-2 on the brain. Human Genetics, 1-10. doi:10.1007/s00439-023-02549-x
NLM
Peron JPS. Direct and indirect impact of SARS-CoV-2 on the brain [Internet]. Human Genetics. 2023 ; 1-10.[citado 2024 set. 28 ] Available from: https://doi.org/10.1007/s00439-023-02549-x
Vancouver
Peron JPS. Direct and indirect impact of SARS-CoV-2 on the brain [Internet]. Human Genetics. 2023 ; 1-10.[citado 2024 set. 28 ] Available from: https://doi.org/10.1007/s00439-023-02549-x
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
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
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: 28 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. 28 ] 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. 28 ] 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
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
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: 28 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. 28 ] 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. 28 ] Available from: https://doi.org/10.1007/s00439-021-02354-4
Artigo de periodico
A novel homozygous RTEL1 variant in a consanguineous Lebanese family: phenotypic heterogeneity and disease anticipation (2019)
Gutierrez-Rodrigues, Fernanda ; Masri, Nohad; Chouery, Eliane; Diamond, Carrie; Jalkh, Nadine; Vicente, Alana; Kajigaya, Sachiko; Abillama, Fayez; Bejjani, Noha; Serhal, Wassim; Calado, Rodrigo Tocantins ; Young, Neal S.; Farhat, Hussein; Coussa, Marie Louise
Source: Human Genetics. Unidade: FMRP
Subjects: HEMATOLOGIA, TELÔMERO, FENÓTIPOS, GENÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
GUTIERREZ-RODRIGUES, Fernanda et al. A novel homozygous RTEL1 variant in a consanguineous Lebanese family: phenotypic heterogeneity and disease anticipation. Human Genetics, v. 138, n. 11-12, p. 1323-1330, 2019Tradução . . Disponível em: https://doi.org/10.1007/s00439-019-02076-8. Acesso em: 28 set. 2024.
APA
Gutierrez-Rodrigues, F., Masri, N., Chouery, E., Diamond, C., Jalkh, N., Vicente, A., et al. (2019). A novel homozygous RTEL1 variant in a consanguineous Lebanese family: phenotypic heterogeneity and disease anticipation. Human Genetics, 138( 11-12), 1323-1330. doi:10.1007/s00439-019-02076-8
NLM
Gutierrez-Rodrigues F, Masri N, Chouery E, Diamond C, Jalkh N, Vicente A, Kajigaya S, Abillama F, Bejjani N, Serhal W, Calado RT, Young NS, Farhat H, Coussa ML. A novel homozygous RTEL1 variant in a consanguineous Lebanese family: phenotypic heterogeneity and disease anticipation [Internet]. Human Genetics. 2019 ; 138( 11-12): 1323-1330.[citado 2024 set. 28 ] Available from: https://doi.org/10.1007/s00439-019-02076-8
Vancouver
Gutierrez-Rodrigues F, Masri N, Chouery E, Diamond C, Jalkh N, Vicente A, Kajigaya S, Abillama F, Bejjani N, Serhal W, Calado RT, Young NS, Farhat H, Coussa ML. A novel homozygous RTEL1 variant in a consanguineous Lebanese family: phenotypic heterogeneity and disease anticipation [Internet]. Human Genetics. 2019 ; 138( 11-12): 1323-1330.[citado 2024 set. 28 ] Available from: https://doi.org/10.1007/s00439-019-02076-8
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
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
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: 28 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. 28 ] 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. 28 ] 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
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
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: 28 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. 28 ]
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. 28 ]
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
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
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: 28 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. 28 ] 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. 28 ] 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
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
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: 28 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. 28 ] 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. 28 ] Available from: https://doi.org/10.1007/s00439-005-0100-2
Artigo de periodico
Absence of the 'delta'ccr5 mutation in indigenous populations of the Brazilian Amazon (1999)
Leboute, Ana Paula M; Carvalho, Mônica W P de; Simões, Aguinaldo Luiz
Source: Human Genetics. Unidade: FMRP
Subjects: GENÉTICA MÉDICA, ÍNDIOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
LEBOUTE, Ana Paula M e CARVALHO, Mônica W P de e SIMÕES, Aguinaldo Luiz. Absence of the 'delta'ccr5 mutation in indigenous populations of the Brazilian Amazon. Human Genetics, v. 105, p. 442-443, 1999Tradução . . Acesso em: 28 set. 2024.
APA
Leboute, A. P. M., Carvalho, M. W. P. de, & Simões, A. L. (1999). Absence of the 'delta'ccr5 mutation in indigenous populations of the Brazilian Amazon. Human Genetics, 105, 442-443.
NLM
Leboute APM, Carvalho MWP de, Simões AL. Absence of the 'delta'ccr5 mutation in indigenous populations of the Brazilian Amazon. Human Genetics. 1999 ; 105 442-443.[citado 2024 set. 28 ]
Vancouver
Leboute APM, Carvalho MWP de, Simões AL. Absence of the 'delta'ccr5 mutation in indigenous populations of the Brazilian Amazon. Human Genetics. 1999 ; 105 442-443.[citado 2024 set. 28 ]
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
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
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: 28 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. 28 ] 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. 28 ] 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
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
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: 28 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. 28 ] 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. 28 ] 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
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
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: 28 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. 28 ] 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. 28 ] Available from: https://doi.org/10.1007/s004390050141
Artigo de periodico
Sry-negative true hermaphrodites and an xx male in two generations of the same family (1996)
Ramos, Ester Silveira; Moreira-Filho, Carlos Alberto; Vicente, Yvone Avalloni M. V. de Andrade; Llorach Velludo, Maria Angeles Sanches; Tucci Júnior, Silvio; Duarte, M H O; Araújo, A G; Martelli, L R
Source: Human Genetics. Unidades: FMRP, ICB
Assunto: IMUNOLOGIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
RAMOS, Ester Silveira et al. Sry-negative true hermaphrodites and an xx male in two generations of the same family. Human Genetics, v. 97, n. 5 , p. 596-8, 1996Tradução . . Disponível em: https://doi.org/10.1007/bf02281867. Acesso em: 28 set. 2024.
APA
Ramos, E. S., Moreira-Filho, C. A., Vicente, Y. A. M. V. de A., Llorach Velludo, M. A. S., Tucci Júnior, S., Duarte, M. H. O., et al. (1996). Sry-negative true hermaphrodites and an xx male in two generations of the same family. Human Genetics, 97( 5 ), 596-8. doi:10.1007/bf02281867
NLM
Ramos ES, Moreira-Filho CA, Vicente YAMV de A, Llorach Velludo MAS, Tucci Júnior S, Duarte MHO, Araújo AG, Martelli LR. Sry-negative true hermaphrodites and an xx male in two generations of the same family [Internet]. Human Genetics. 1996 ;97( 5 ): 596-8.[citado 2024 set. 28 ] Available from: https://doi.org/10.1007/bf02281867
Vancouver
Ramos ES, Moreira-Filho CA, Vicente YAMV de A, Llorach Velludo MAS, Tucci Júnior S, Duarte MHO, Araújo AG, Martelli LR. Sry-negative true hermaphrodites and an xx male in two generations of the same family [Internet]. Human Genetics. 1996 ;97( 5 ): 596-8.[citado 2024 set. 28 ] Available from: https://doi.org/10.1007/bf02281867
Artigo de periodico
Xy gonadal dysgenesis and gonadoblastoma: a study in two sisters with a cryptic deletion of the y chromosome involving the sry gene (1995)
Barbosa, A S; Ferraz Costa, T E; Semer, M; Liberman, Bernardo; Moreira-Filho, Carlos Alberto
Source: Human Genetics. Unidade: ICB
Assunto: IMUNOLOGIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
BARBOSA, A S et al. Xy gonadal dysgenesis and gonadoblastoma: a study in two sisters with a cryptic deletion of the y chromosome involving the sry gene. Human Genetics, v. 95, p. 63-6, 1995Tradução . . Disponível em: https://doi.org/10.1007/bf00225076. Acesso em: 28 set. 2024.
APA
Barbosa, A. S., Ferraz Costa, T. E., Semer, M., Liberman, B., & Moreira-Filho, C. A. (1995). Xy gonadal dysgenesis and gonadoblastoma: a study in two sisters with a cryptic deletion of the y chromosome involving the sry gene. Human Genetics, 95, 63-6. doi:10.1007/bf00225076
NLM
Barbosa AS, Ferraz Costa TE, Semer M, Liberman B, Moreira-Filho CA. Xy gonadal dysgenesis and gonadoblastoma: a study in two sisters with a cryptic deletion of the y chromosome involving the sry gene [Internet]. Human Genetics. 1995 ;95 63-6.[citado 2024 set. 28 ] Available from: https://doi.org/10.1007/bf00225076
Vancouver
Barbosa AS, Ferraz Costa TE, Semer M, Liberman B, Moreira-Filho CA. Xy gonadal dysgenesis and gonadoblastoma: a study in two sisters with a cryptic deletion of the y chromosome involving the sry gene [Internet]. Human Genetics. 1995 ;95 63-6.[citado 2024 set. 28 ] Available from: https://doi.org/10.1007/bf00225076
Artigo de periodico
Beta-globin gene cluster haplotypes in yanomama indians from the amazon region of brazil (1992)
Guerreiro, J F; Figueiredo, Mauro Silvério; Santos, S. E. B.
Source: Human Genetics. Unidade: FMRP
Subjects: GENÉTICA, GENÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
GUERREIRO, J F e FIGUEIREDO, Mauro Silvério e SANTOS, S. E. B. Beta-globin gene cluster haplotypes in yanomama indians from the amazon region of brazil. Human Genetics, v. 89, p. 629-31, 1992Tradução . . Acesso em: 28 set. 2024.
APA
Guerreiro, J. F., Figueiredo, M. S., & Santos, S. E. B. (1992). Beta-globin gene cluster haplotypes in yanomama indians from the amazon region of brazil. Human Genetics, 89, 629-31.
NLM
Guerreiro JF, Figueiredo MS, Santos SEB. Beta-globin gene cluster haplotypes in yanomama indians from the amazon region of brazil. Human Genetics. 1992 ;89 629-31.[citado 2024 set. 28 ]
Vancouver
Guerreiro JF, Figueiredo MS, Santos SEB. Beta-globin gene cluster haplotypes in yanomama indians from the amazon region of brazil. Human Genetics. 1992 ;89 629-31.[citado 2024 set. 28 ]
Artigo de periodico
Hemoglobin stanleyville ii (alpha 78 asn-lys) s associated with a 37-kb alpha-globin (1991)
Costa, F F; Sonati, M F; Zago, M A
Source: Human Genetics. Unidade: FMRP
Assunto: GENÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
COSTA, F F e SONATI, M F e ZAGO, M A. Hemoglobin stanleyville ii (alpha 78 asn-lys) s associated with a 37-kb alpha-globin. Human Genetics, v. 86, p. 319-20, 1991Tradução . . Acesso em: 28 set. 2024.
APA
Costa, F. F., Sonati, M. F., & Zago, M. A. (1991). Hemoglobin stanleyville ii (alpha 78 asn-lys) s associated with a 37-kb alpha-globin. Human Genetics, 86, 319-20.
NLM
Costa FF, Sonati MF, Zago MA. Hemoglobin stanleyville ii (alpha 78 asn-lys) s associated with a 37-kb alpha-globin. Human Genetics. 1991 ;86 319-20.[citado 2024 set. 28 ]
Vancouver
Costa FF, Sonati MF, Zago MA. Hemoglobin stanleyville ii (alpha 78 asn-lys) s associated with a 37-kb alpha-globin. Human Genetics. 1991 ;86 319-20.[citado 2024 set. 28 ]
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
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
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: 28 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. 28 ] 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. 28 ] Available from: https://doi.org/10.1007/bf01213107
Artigo de periodico
Investigation of the zfy gene in xx true hermaphroditism and swyer syndrome (1990)
Damiani, D; Billerbeck, A E C; Goldberg, A C K; Setian, Nuvarte; Fellous, M; Kalil Filho, Jorge Elias
Source: Human Genetics. Unidade: FM
Assunto: ENDOCRINOLOGIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
DAMIANI, D et al. Investigation of the zfy gene in xx true hermaphroditism and swyer syndrome. Human Genetics, v. 85, p. 85-8, 1990Tradução . . Acesso em: 28 set. 2024.
APA
Damiani, D., Billerbeck, A. E. C., Goldberg, A. C. K., Setian, N., Fellous, M., & Kalil Filho, J. E. (1990). Investigation of the zfy gene in xx true hermaphroditism and swyer syndrome. Human Genetics, 85, 85-8.
NLM
Damiani D, Billerbeck AEC, Goldberg ACK, Setian N, Fellous M, Kalil Filho JE. Investigation of the zfy gene in xx true hermaphroditism and swyer syndrome. Human Genetics. 1990 ;85 85-8.[citado 2024 set. 28 ]
Vancouver
Damiani D, Billerbeck AEC, Goldberg ACK, Setian N, Fellous M, Kalil Filho JE. Investigation of the zfy gene in xx true hermaphroditism and swyer syndrome. Human Genetics. 1990 ;85 85-8.[citado 2024 set. 28 ]
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
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
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: 28 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. 28 ] 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. 28 ] Available from: https://doi.org/10.1007/bf00197693
Artigo de periodico
Gd (+) cuiaba, a new rare glucose -6- phosphate dehydrogenase variant presenting normal activity (1987)
Barretto, Orlando César de Oliveira; Nonoyama, K.
Source: Human Genetics. Unidade: FM
Assunto: MEDICINA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
BARRETTO, Orlando César de Oliveira e NONOYAMA, K. Gd (+) cuiaba, a new rare glucose -6- phosphate dehydrogenase variant presenting normal activity. Human Genetics, v. 77, p. 201-202, 1987Tradução . . Disponível em: https://doi.org/10.1007/bf00272394. Acesso em: 28 set. 2024.
APA
Barretto, O. C. de O., & Nonoyama, K. (1987). Gd (+) cuiaba, a new rare glucose -6- phosphate dehydrogenase variant presenting normal activity. Human Genetics, 77, 201-202. doi:10.1007/bf00272394
NLM
Barretto OC de O, Nonoyama K. Gd (+) cuiaba, a new rare glucose -6- phosphate dehydrogenase variant presenting normal activity [Internet]. Human Genetics. 1987 ; 77 201-202.[citado 2024 set. 28 ] Available from: https://doi.org/10.1007/bf00272394
Vancouver
Barretto OC de O, Nonoyama K. Gd (+) cuiaba, a new rare glucose -6- phosphate dehydrogenase variant presenting normal activity [Internet]. Human Genetics. 1987 ; 77 201-202.[citado 2024 set. 28 ] Available from: https://doi.org/10.1007/bf00272394

USP Schools

ReP

Filtros

Departament

Authors

USP affiliated authors

Date published

Subjects

Funding Agencies

Indexado em

Non normalized affiliation