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Artigo de periodico
A novel autosomal dominant deafness locus (DFNA58) maps to 2p12-p21 (2009)
Lezirovitz, Karina; Braga, M. C. C.; Thiele-Aguiar, Renata Soares; Auricchio, Maria Teresa Ballester de Melo; Pearson, Peter Lees; Otto, Paulo A ; Mingroni Netto, Regina Celia
Source: Clinical Genetics. Unidade: IB
Subjects: MUTAÇÃO GENÉTICA, DOENÇAS HEREDITÁRIAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
LEZIROVITZ, Karina et al. A novel autosomal dominant deafness locus (DFNA58) maps to 2p12-p21. Clinical Genetics, v. 75, n. 5, p. 490-493, 2009Tradução . . Acesso em: 14 nov. 2024.
APA
Lezirovitz, K., Braga, M. C. C., Thiele-Aguiar, R. S., Auricchio, M. T. B. de M., Pearson, P. L., Otto, P. A., & Mingroni Netto, R. C. (2009). A novel autosomal dominant deafness locus (DFNA58) maps to 2p12-p21. Clinical Genetics, 75( 5), 490-493.
NLM
Lezirovitz K, Braga MCC, Thiele-Aguiar RS, Auricchio MTB de M, Pearson PL, Otto PA, Mingroni Netto RC. A novel autosomal dominant deafness locus (DFNA58) maps to 2p12-p21. Clinical Genetics. 2009 ; 75( 5): 490-493.[citado 2024 nov. 14 ]
Vancouver
Lezirovitz K, Braga MCC, Thiele-Aguiar RS, Auricchio MTB de M, Pearson PL, Otto PA, Mingroni Netto RC. A novel autosomal dominant deafness locus (DFNA58) maps to 2p12-p21. Clinical Genetics. 2009 ; 75( 5): 490-493.[citado 2024 nov. 14 ]
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: 14 nov. 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 nov. 14 ]
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 nov. 14 ]
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: 14 nov. 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 nov. 14 ] 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 nov. 14 ] Available from: https://doi.org/10.1007/s00439-008-0515-7
Artigo de periodico
Whole-genome array-CGH screening in undiagnosed syndromic patients: old syndromes revisited and new alterations (2006)
Krepischi, Ana Cristina Victorino ; Vianna-Morgante, Angela M ; Jehee, Fernanda Sarquis; Passos-Bueno, Maria Rita ; Knijnenburg, Jeroen; Szuhai, K.; Sloos, W.; Mazzeu, Juliana Forte; Kok, Fernando; Cheroki, C.; Otto, Paulo A ; Mingroni Netto, Regina Celia ; Varela, Monica Castro; Koiffmann, Celia Priszkulnik ; Kim, Chong A.; Bertola, Débora Romeo; Pearson, Peter Lees
Source: Cytogenetic and Genome Research. Unidade: IB
Assunto: ANORMALIDADES CROMOSSÔMICAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
KREPISCHI, Ana Cristina Victorino et al. Whole-genome array-CGH screening in undiagnosed syndromic patients: old syndromes revisited and new alterations. Cytogenetic and Genome Research, v. 115, n. 3-4, p. 254-261, 2006Tradução . . Disponível em: https://doi.org/10.1159/000095922. Acesso em: 14 nov. 2024.
APA
Krepischi, A. C. V., Vianna-Morgante, A. M., Jehee, F. S., Passos-Bueno, M. R., Knijnenburg, J., Szuhai, K., et al. (2006). Whole-genome array-CGH screening in undiagnosed syndromic patients: old syndromes revisited and new alterations. Cytogenetic and Genome Research, 115( 3-4), 254-261. doi:10.1159/000095922
NLM
Krepischi ACV, Vianna-Morgante AM, Jehee FS, Passos-Bueno MR, Knijnenburg J, Szuhai K, Sloos W, Mazzeu JF, Kok F, Cheroki C, Otto PA, Mingroni Netto RC, Varela MC, Koiffmann CP, Kim CA, Bertola DR, Pearson PL. Whole-genome array-CGH screening in undiagnosed syndromic patients: old syndromes revisited and new alterations [Internet]. Cytogenetic and Genome Research. 2006 ; 115( 3-4): 254-261.[citado 2024 nov. 14 ] Available from: https://doi.org/10.1159/000095922
Vancouver
Krepischi ACV, Vianna-Morgante AM, Jehee FS, Passos-Bueno MR, Knijnenburg J, Szuhai K, Sloos W, Mazzeu JF, Kok F, Cheroki C, Otto PA, Mingroni Netto RC, Varela MC, Koiffmann CP, Kim CA, Bertola DR, Pearson PL. Whole-genome array-CGH screening in undiagnosed syndromic patients: old syndromes revisited and new alterations [Internet]. Cytogenetic and Genome Research. 2006 ; 115( 3-4): 254-261.[citado 2024 nov. 14 ] Available from: https://doi.org/10.1159/000095922

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