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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
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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
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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: 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
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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: 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
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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
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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: 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
Linkage to chromosome 2q36.1 in autosomal dominant Dandy-Walker malformation with occipital cephalocele and evidence for genetic heterogeneity (2008)
Jalali, Ali; Aldinger, Kimberly A.; Chary, Ajit; McLone, David G.; Bowman, Robin M.; Le, Luan Cong; Jardine, Phillip; Newbury-Ecob, Ruth; Mallick, Andrew; Jafari, Nadereh; Russell, Eric J.; Curran, John; Nguyen, Pam; Ouahchi, Karim; Lee, Charles; Dobyns, William B.; Millen, Kathleen J.; Pina Neto, João Monteiro; Kessler, John A.; Bassuk, Alexander G.
Source: Human Genetics. Unidade: FMRP
Subjects: GENÉTICA MÉDICA, NEUROLOGIA
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JALALI, Ali et al. Linkage to chromosome 2q36.1 in autosomal dominant Dandy-Walker malformation with occipital cephalocele and evidence for genetic heterogeneity. Human Genetics, v. 123, n. 3, p. 237-245, 2008Tradução . . Disponível em: https://doi.org/10.1007/s00439-008-0467-y. Acesso em: 28 set. 2024.
APA
Jalali, A., Aldinger, K. A., Chary, A., McLone, D. G., Bowman, R. M., Le, L. C., et al. (2008). Linkage to chromosome 2q36.1 in autosomal dominant Dandy-Walker malformation with occipital cephalocele and evidence for genetic heterogeneity. Human Genetics, 123( 3), 237-245. doi:10.1007/s00439-008-0467-y
NLM
Jalali A, Aldinger KA, Chary A, McLone DG, Bowman RM, Le LC, Jardine P, Newbury-Ecob R, Mallick A, Jafari N, Russell EJ, Curran J, Nguyen P, Ouahchi K, Lee C, Dobyns WB, Millen KJ, Pina Neto JM, Kessler JA, Bassuk AG. Linkage to chromosome 2q36.1 in autosomal dominant Dandy-Walker malformation with occipital cephalocele and evidence for genetic heterogeneity [Internet]. Human Genetics. 2008 ; 123( 3): 237-245.[citado 2024 set. 28 ] Available from: https://doi.org/10.1007/s00439-008-0467-y
Vancouver
Jalali A, Aldinger KA, Chary A, McLone DG, Bowman RM, Le LC, Jardine P, Newbury-Ecob R, Mallick A, Jafari N, Russell EJ, Curran J, Nguyen P, Ouahchi K, Lee C, Dobyns WB, Millen KJ, Pina Neto JM, Kessler JA, Bassuk AG. Linkage to chromosome 2q36.1 in autosomal dominant Dandy-Walker malformation with occipital cephalocele and evidence for genetic heterogeneity [Internet]. Human Genetics. 2008 ; 123( 3): 237-245.[citado 2024 set. 28 ] Available from: https://doi.org/10.1007/s00439-008-0467-y
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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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
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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: 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
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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: 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
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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
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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
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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: 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
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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
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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
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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

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