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Artigo de periodico
DNA methylation landscape of hepatoblastomas reveals arrest at early stages of liver differentiation and cancer-related alterations (2017)
Maschietto, Mariana; Rodrigues, Tatiane Cristina; Kashiwabara, André Yoshiaki; Araújo, Érica Sara Souza de; Aguiar, Talita Ferreira Marques; Costa, Cecília Maria Lima da; Cunha, Isabela Werneck da; Vasques, Luciana dos Reis; Cypriano, Monica; Brentani, Helena; Toledo, Silvia Regina Caminada de; Pearson, Peter Lees; Carraro, Dirce Maria; Rosenberg, Carla ; Krepischi, Ana Cristina Victorino
Fonte: Oncotarget. Unidades: FM, IB
Assuntos: NEOPLASIAS HEPÁTICAS, CITOGENÉTICA, METILAÇÃO DE DNA, DIFERENCIAÇÃO CELULAR, EXPRESSÃO GÊNICA, GENÉTICA MÉDICA
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ABNT
MASCHIETTO, Mariana et al. DNA methylation landscape of hepatoblastomas reveals arrest at early stages of liver differentiation and cancer-related alterations. Oncotarget, v. No 2017, n. 58, p. 97871-97889, 2017Tradução . . Disponível em: https://doi.org/10.18632/oncotarget.14208. Acesso em: 21 out. 2025.
APA
Maschietto, M., Rodrigues, T. C., Kashiwabara, A. Y., Araújo, É. S. S. de, Aguiar, T. F. M., Costa, C. M. L. da, et al. (2017). DNA methylation landscape of hepatoblastomas reveals arrest at early stages of liver differentiation and cancer-related alterations. Oncotarget, No 2017( 58), 97871-97889. doi:10.18632/oncotarget.14208
NLM
Maschietto M, Rodrigues TC, Kashiwabara AY, Araújo ÉSS de, Aguiar TFM, Costa CML da, Cunha IW da, Vasques L dos R, Cypriano M, Brentani H, Toledo SRC de, Pearson PL, Carraro DM, Rosenberg C, Krepischi ACV. DNA methylation landscape of hepatoblastomas reveals arrest at early stages of liver differentiation and cancer-related alterations [Internet]. Oncotarget. 2017 ; No 2017( 58): 97871-97889.[citado 2025 out. 21 ] Available from: https://doi.org/10.18632/oncotarget.14208
Vancouver
Maschietto M, Rodrigues TC, Kashiwabara AY, Araújo ÉSS de, Aguiar TFM, Costa CML da, Cunha IW da, Vasques L dos R, Cypriano M, Brentani H, Toledo SRC de, Pearson PL, Carraro DM, Rosenberg C, Krepischi ACV. DNA methylation landscape of hepatoblastomas reveals arrest at early stages of liver differentiation and cancer-related alterations [Internet]. Oncotarget. 2017 ; No 2017( 58): 97871-97889.[citado 2025 out. 21 ] Available from: https://doi.org/10.18632/oncotarget.14208
Artigo de periodico
Thiazole Orange as an Alternative to Antibody Binding for Detecting Triple-helical DNA in Heterochromatin of Drosophila and Rhynchosciara (2017)
Gorab, Eduardo; Pearson, Peter Lees
Fonte: Journal of Histochemistry & Cytochemistry. Unidade: IB
Assuntos: GENÉTICA ANIMAL, CITOGENÉTICA, ANTICORPOS, CROMOSSOMOS, CROMATINA, DROSOPHILA, INSETOS, DIPTERA
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GORAB, Eduardo e PEARSON, Peter Lees. Thiazole Orange as an Alternative to Antibody Binding for Detecting Triple-helical DNA in Heterochromatin of Drosophila and Rhynchosciara. Journal of Histochemistry & Cytochemistry, p. 1-12, 2017Tradução . . Disponível em: https://doi.org/10.1369/0022155417745496. Acesso em: 21 out. 2025.
APA
Gorab, E., & Pearson, P. L. (2017). Thiazole Orange as an Alternative to Antibody Binding for Detecting Triple-helical DNA in Heterochromatin of Drosophila and Rhynchosciara. Journal of Histochemistry & Cytochemistry, 1-12. doi:10.1369/0022155417745496
NLM
Gorab E, Pearson PL. Thiazole Orange as an Alternative to Antibody Binding for Detecting Triple-helical DNA in Heterochromatin of Drosophila and Rhynchosciara [Internet]. Journal of Histochemistry & Cytochemistry. 2017 ; 1-12.[citado 2025 out. 21 ] Available from: https://doi.org/10.1369/0022155417745496
Vancouver
Gorab E, Pearson PL. Thiazole Orange as an Alternative to Antibody Binding for Detecting Triple-helical DNA in Heterochromatin of Drosophila and Rhynchosciara [Internet]. Journal of Histochemistry & Cytochemistry. 2017 ; 1-12.[citado 2025 out. 21 ] Available from: https://doi.org/10.1369/0022155417745496
Artigo de periodico
Large germline copy number variations as predisposing factor in childhood neoplasms (2014)
Krepischi, Ana Cristina Victorino ; Capelli, Leonardo Pires; Silva, Amanda Gonçalves; Araújo, Érica Sara Souza de; Pearson, Peter Lees; Heck, Benjamin; Costa, Cecília Maria Lima da; Camargo, Beatriz de; Rosenberg, Carla
Fonte: Future Oncology. Unidade: IB
Assuntos: NEOPLASIAS, INFÂNCIA, GENÉTICA (FATORES), CROMOSSOMOS, GENÉTICA MÉDICA, ONCOLOGIA
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KREPISCHI, Ana Cristina Victorino et al. Large germline copy number variations as predisposing factor in childhood neoplasms. Future Oncology, v. 10, n. 9, p. 1627-1633, 2014Tradução . . Disponível em: https://doi.org/10.2217/FON.14.41. Acesso em: 21 out. 2025.
APA
Krepischi, A. C. V., Capelli, L. P., Silva, A. G., Araújo, É. S. S. de, Pearson, P. L., Heck, B., et al. (2014). Large germline copy number variations as predisposing factor in childhood neoplasms. Future Oncology, 10( 9), 1627-1633. doi:10.2217/FON.14.41
NLM
Krepischi ACV, Capelli LP, Silva AG, Araújo ÉSS de, Pearson PL, Heck B, Costa CML da, Camargo B de, Rosenberg C. Large germline copy number variations as predisposing factor in childhood neoplasms [Internet]. Future Oncology. 2014 ; 10( 9): 1627-1633.[citado 2025 out. 21 ] Available from: https://doi.org/10.2217/FON.14.41
Vancouver
Krepischi ACV, Capelli LP, Silva AG, Araújo ÉSS de, Pearson PL, Heck B, Costa CML da, Camargo B de, Rosenberg C. Large germline copy number variations as predisposing factor in childhood neoplasms [Internet]. Future Oncology. 2014 ; 10( 9): 1627-1633.[citado 2025 out. 21 ] Available from: https://doi.org/10.2217/FON.14.41
Artigo de periodico
Number of rare germline CNVs and TP53 mutation types (2012)
Silva, Amanda G; Achatz, Maria Isabel W; Krepischi, Ana Cristina Victorino ; Pearson, Peter Lees; Rosenberg, Carla
Fonte: Orphanet Journal of Rare Diseases. Unidade: IB
Assuntos: GENÉTICA, MUTAÇÃO GENÉTICA, NEOPLASIAS
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ABNT
SILVA, Amanda G et al. Number of rare germline CNVs and TP53 mutation types. Orphanet Journal of Rare Diseases, v. 7, p. on-line, 2012Tradução . . Disponível em: https://doi.org/10.1186/1750-1172-7-101. Acesso em: 21 out. 2025.
APA
Silva, A. G., Achatz, M. I. W., Krepischi, A. C. V., Pearson, P. L., & Rosenberg, C. (2012). Number of rare germline CNVs and TP53 mutation types. Orphanet Journal of Rare Diseases, 7, on-line. doi:10.1186/1750-1172-7-101
NLM
Silva AG, Achatz MIW, Krepischi ACV, Pearson PL, Rosenberg C. Number of rare germline CNVs and TP53 mutation types [Internet]. Orphanet Journal of Rare Diseases. 2012 ; 7 on-line.[citado 2025 out. 21 ] Available from: https://doi.org/10.1186/1750-1172-7-101
Vancouver
Silva AG, Achatz MIW, Krepischi ACV, Pearson PL, Rosenberg C. Number of rare germline CNVs and TP53 mutation types [Internet]. Orphanet Journal of Rare Diseases. 2012 ; 7 on-line.[citado 2025 out. 21 ] Available from: https://doi.org/10.1186/1750-1172-7-101
Artigo de periodico
Germline copy number variations and cancer predisposition (2012)
Krepischi, Ana Cristina Victorino ; Pearson, Peter Lees; Rosenberg, Carla
Fonte: Future Oncology. Unidade: IB
Assuntos: NEOPLASIAS, GENES, DOENÇAS GENÉTICAS
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ABNT
KREPISCHI, Ana Cristina Victorino e PEARSON, Peter Lees e ROSENBERG, Carla. Germline copy number variations and cancer predisposition. Future Oncology, v. 8, n. 4, p. 441-450, 2012Tradução . . Disponível em: https://doi.org/10.2217/fon.12.34. Acesso em: 21 out. 2025.
APA
Krepischi, A. C. V., Pearson, P. L., & Rosenberg, C. (2012). Germline copy number variations and cancer predisposition. Future Oncology, 8( 4), 441-450. doi:10.2217/fon.12.34
NLM
Krepischi ACV, Pearson PL, Rosenberg C. Germline copy number variations and cancer predisposition [Internet]. Future Oncology. 2012 ; 8( 4): 441-450.[citado 2025 out. 21 ] Available from: https://doi.org/10.2217/fon.12.34
Vancouver
Krepischi ACV, Pearson PL, Rosenberg C. Germline copy number variations and cancer predisposition [Internet]. Future Oncology. 2012 ; 8( 4): 441-450.[citado 2025 out. 21 ] Available from: https://doi.org/10.2217/fon.12.34
Artigo de periodico
Human stem cell cultures from cleft lip/palate patients show enrichment of transcripts involved in extracellular matrix modeling by comparison to controls (2011)
Bueno, Daniela Franco; Sunaga, Daniele Yumi; Kobayashi, Gerson Shigeru; Aguena, Meire; Raposo-Amaral, Cassio Eduardo; Masotti, Cibele; Cruz, Lucas Alvizi; Pearson, Peter Lees; Passos-Bueno, Maria Rita
Fonte: Stem Cell Reviews and Reports. Unidade: IB
Assuntos: GENÉTICA, LÁBIO FISSURADO, CÉLULAS-TRONCO
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ABNT
BUENO, Daniela Franco et al. Human stem cell cultures from cleft lip/palate patients show enrichment of transcripts involved in extracellular matrix modeling by comparison to controls. Stem Cell Reviews and Reports, v. 7, n. Ju 2011, p. 446-457, 2011Tradução . . Disponível em: https://doi.org/10.1007/s12015-010-9197-3. Acesso em: 21 out. 2025.
APA
Bueno, D. F., Sunaga, D. Y., Kobayashi, G. S., Aguena, M., Raposo-Amaral, C. E., Masotti, C., et al. (2011). Human stem cell cultures from cleft lip/palate patients show enrichment of transcripts involved in extracellular matrix modeling by comparison to controls. Stem Cell Reviews and Reports, 7( Ju 2011), 446-457. doi:10.1007/s12015-010-9197-3
NLM
Bueno DF, Sunaga DY, Kobayashi GS, Aguena M, Raposo-Amaral CE, Masotti C, Cruz LA, Pearson PL, Passos-Bueno MR. Human stem cell cultures from cleft lip/palate patients show enrichment of transcripts involved in extracellular matrix modeling by comparison to controls [Internet]. Stem Cell Reviews and Reports. 2011 ;7( Ju 2011): 446-457.[citado 2025 out. 21 ] Available from: https://doi.org/10.1007/s12015-010-9197-3
Vancouver
Bueno DF, Sunaga DY, Kobayashi GS, Aguena M, Raposo-Amaral CE, Masotti C, Cruz LA, Pearson PL, Passos-Bueno MR. Human stem cell cultures from cleft lip/palate patients show enrichment of transcripts involved in extracellular matrix modeling by comparison to controls [Internet]. Stem Cell Reviews and Reports. 2011 ;7( Ju 2011): 446-457.[citado 2025 out. 21 ] Available from: https://doi.org/10.1007/s12015-010-9197-3
Artigo de periodico
Two distinct regions in 2q24.2-q24.3 associated with idiopathic epilepsy (2010)
Krepischi, Ana Cristina Victorino ; Knijnenburg, Jeroen; Bertola, Debora Romeu; Kim, Chong Ae; Pearson, Peter Lees; Bijlsma, Emilia; Szuhai, Karoly; Kok, Fernando; Vianna-Morgante, Angela M ; Rosenberg, Carla
Fonte: Epilepsia. Unidade: IB
Assuntos: EPILEPSIA, GENÉTICA, NEUROLOGIA
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ABNT
KREPISCHI, Ana Cristina Victorino et al. Two distinct regions in 2q24.2-q24.3 associated with idiopathic epilepsy. Epilepsia, v. 51 n. 12, p. 2457-2460, 2010Tradução . . Disponível em: https://doi.org/10.1111/j.1528-1167.2010.02742.x. Acesso em: 21 out. 2025.
APA
Krepischi, A. C. V., Knijnenburg, J., Bertola, D. R., Kim, C. A., Pearson, P. L., Bijlsma, E., et al. (2010). Two distinct regions in 2q24.2-q24.3 associated with idiopathic epilepsy. Epilepsia, 51 n. 12, 2457-2460. doi:10.1111/j.1528-1167.2010.02742.x
NLM
Krepischi ACV, Knijnenburg J, Bertola DR, Kim CA, Pearson PL, Bijlsma E, Szuhai K, Kok F, Vianna-Morgante AM, Rosenberg C. Two distinct regions in 2q24.2-q24.3 associated with idiopathic epilepsy [Internet]. Epilepsia. 2010 ; 51 n. 12 2457-2460.[citado 2025 out. 21 ] Available from: https://doi.org/10.1111/j.1528-1167.2010.02742.x
Vancouver
Krepischi ACV, Knijnenburg J, Bertola DR, Kim CA, Pearson PL, Bijlsma E, Szuhai K, Kok F, Vianna-Morgante AM, Rosenberg C. Two distinct regions in 2q24.2-q24.3 associated with idiopathic epilepsy [Internet]. Epilepsia. 2010 ; 51 n. 12 2457-2460.[citado 2025 out. 21 ] Available from: https://doi.org/10.1111/j.1528-1167.2010.02742.x
Artigo de periodico
Genetic variability in the myostatin gene does not explain the muscle hypertrophy and clinical penetrance in myotonia congenita (2010)
Muniz, Viviane Palhares; Senkevics, Adriano S; Zilbersztajn, Dinorah; Gurgel-Giannetti, Juliana; Silva, Helga Cristina Almeida da; Yamamoto, Lydia Uraco; Pavanello, Rita C. M; Pearson, Peter Lees; Zatz, Mayana ; Vainzof, Mariz
Fonte: Muscle & Nerve. Unidade: IB
Assuntos: VARIAÇÃO GENÉTICA, MÚSCULO ESQUELÉTICO
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ABNT
MUNIZ, Viviane Palhares et al. Genetic variability in the myostatin gene does not explain the muscle hypertrophy and clinical penetrance in myotonia congenita. Muscle & Nerve, v. 41, n. 3, p. 427-428, 2010Tradução . . Disponível em: https://doi.org/10.1002/MUS21627. Acesso em: 21 out. 2025.
APA
Muniz, V. P., Senkevics, A. S., Zilbersztajn, D., Gurgel-Giannetti, J., Silva, H. C. A. da, Yamamoto, L. U., et al. (2010). Genetic variability in the myostatin gene does not explain the muscle hypertrophy and clinical penetrance in myotonia congenita. Muscle & Nerve, 41( 3), 427-428. doi:10.1002/MUS21627
NLM
Muniz VP, Senkevics AS, Zilbersztajn D, Gurgel-Giannetti J, Silva HCA da, Yamamoto LU, Pavanello RCM, Pearson PL, Zatz M, Vainzof M. Genetic variability in the myostatin gene does not explain the muscle hypertrophy and clinical penetrance in myotonia congenita [Internet]. Muscle & Nerve. 2010 ; 41( 3): 427-428.[citado 2025 out. 21 ] Available from: https://doi.org/10.1002/MUS21627
Vancouver
Muniz VP, Senkevics AS, Zilbersztajn D, Gurgel-Giannetti J, Silva HCA da, Yamamoto LU, Pavanello RCM, Pearson PL, Zatz M, Vainzof M. Genetic variability in the myostatin gene does not explain the muscle hypertrophy and clinical penetrance in myotonia congenita [Internet]. Muscle & Nerve. 2010 ; 41( 3): 427-428.[citado 2025 out. 21 ] Available from: https://doi.org/10.1002/MUS21627
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
Fonte: Clinical Genetics. Unidade: IB
Assuntos: MUTAÇÃO GENÉTICA, DOENÇAS HEREDITÁRIAS
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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: 21 out. 2025.
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 2025 out. 21 ]
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 2025 out. 21 ]
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
Fonte: Human Genetics. Unidade: IB
Assuntos: 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: 21 out. 2025.
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 2025 out. 21 ]
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 2025 out. 21 ]
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
Fonte: Human Genetics. Unidade: IB
Assuntos: DOENÇAS GENÉTICAS, MALFORMAÇÕES
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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: 21 out. 2025.
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 2025 out. 21 ] 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 2025 out. 21 ] Available from: https://doi.org/10.1007/s00439-008-0515-7
Artigo de periodico
Ringo, a Golden Retriever muscular dystrophy (GRMD) dog with absent dystrophin but normal strength (2008)
Ambrósio, Carlos Eduardo; Valadares, M. C; Zucconi, E; Cabral, R; Pearson, Peter Lees; Gaiad, Thaís Peixoto; Canovas, Marta; Vainzof, Mariz ; Miglino, Maria Angélica ; Zatz, Mayana
Fonte: Neuromuscular Disorders. Unidades: IB, FMVZ
Assuntos: CÃO GOLDEN RETRIEVER, DISTROFIA MUSCULAR ANIMAL, DOENÇAS MUSCULARES EM ANIMAL
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ABNT
AMBRÓSIO, Carlos Eduardo et al. Ringo, a Golden Retriever muscular dystrophy (GRMD) dog with absent dystrophin but normal strength. Neuromuscular Disorders, v. No 2008, n. 11, p. 892-893, 2008Tradução . . Disponível em: https://doi.org/10.1016/j.nmd.2008.06.385. Acesso em: 21 out. 2025.
APA
Ambrósio, C. E., Valadares, M. C., Zucconi, E., Cabral, R., Pearson, P. L., Gaiad, T. P., et al. (2008). Ringo, a Golden Retriever muscular dystrophy (GRMD) dog with absent dystrophin but normal strength. Neuromuscular Disorders, No 2008( 11), 892-893. doi:10.1016/j.nmd.2008.06.385
NLM
Ambrósio CE, Valadares MC, Zucconi E, Cabral R, Pearson PL, Gaiad TP, Canovas M, Vainzof M, Miglino MA, Zatz M. Ringo, a Golden Retriever muscular dystrophy (GRMD) dog with absent dystrophin but normal strength [Internet]. Neuromuscular Disorders. 2008 ; No 2008( 11): 892-893.[citado 2025 out. 21 ] Available from: https://doi.org/10.1016/j.nmd.2008.06.385
Vancouver
Ambrósio CE, Valadares MC, Zucconi E, Cabral R, Pearson PL, Gaiad TP, Canovas M, Vainzof M, Miglino MA, Zatz M. Ringo, a Golden Retriever muscular dystrophy (GRMD) dog with absent dystrophin but normal strength [Internet]. Neuromuscular Disorders. 2008 ; No 2008( 11): 892-893.[citado 2025 out. 21 ] Available from: https://doi.org/10.1016/j.nmd.2008.06.385
Trabalho de evento-resumo
Clinical variability in Golden retriever muscular dystrophy (GRMD) dogs (2008)
Valadares, M. C.; Ambrósio, Carlos Eduardo; Cabral, R.; Zucconi, E; Pearson, Peter Lees; Gaiad, Thaís Peixoto; Canovas, M.; Vainzof, Mariz ; Araújo, M. S.; Miglino, Maria Angélica ; Zatz, Mayana
Fonte: Resumo. Nome do evento: Congresso Brasileiro de Genética. Unidades: IB, FMVZ
Assunto: DISTROFIA MUSCULAR ANIMAL
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ABNT
VALADARES, M. C. et al. Clinical variability in Golden retriever muscular dystrophy (GRMD) dogs. 2008, Anais.. Salvador: Instituto de Biociências, Universidade de São Paulo, 2008. . Acesso em: 21 out. 2025.
APA
Valadares, M. C., Ambrósio, C. E., Cabral, R., Zucconi, E., Pearson, P. L., Gaiad, T. P., et al. (2008). Clinical variability in Golden retriever muscular dystrophy (GRMD) dogs. In Resumo. Salvador: Instituto de Biociências, Universidade de São Paulo.
NLM
Valadares MC, Ambrósio CE, Cabral R, Zucconi E, Pearson PL, Gaiad TP, Canovas M, Vainzof M, Araújo MS, Miglino MA, Zatz M. Clinical variability in Golden retriever muscular dystrophy (GRMD) dogs. Resumo. 2008 ;[citado 2025 out. 21 ]
Vancouver
Valadares MC, Ambrósio CE, Cabral R, Zucconi E, Pearson PL, Gaiad TP, Canovas M, Vainzof M, Araújo MS, Miglino MA, Zatz M. Clinical variability in Golden retriever muscular dystrophy (GRMD) dogs. Resumo. 2008 ;[citado 2025 out. 21 ]
Trabalho de evento-resumo
Maximum likelyhood estimates of penetrance: a pilot study using the ectrodactyly-hemimelia syndrome (2007)
Horimoto, Andréa Roseli Vançan Russo; Lezirovitz, Karina; Pearson, Peter Lees; Otto, Paulo A
Fonte: Resumo. Nome do evento: Congresso Brasileiro de Genética. Unidade: IB
Assunto: ACONSELHAMENTO GENÉTICO
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ABNT
HORIMOTO, Andréa Roseli Vançan Russo et al. Maximum likelyhood estimates of penetrance: a pilot study using the ectrodactyly-hemimelia syndrome. 2007, Anais.. Águas de Lindóia: Instituto de Biociências, Universidade de São Paulo, 2007. . Acesso em: 21 out. 2025.
APA
Horimoto, A. R. V. R., Lezirovitz, K., Pearson, P. L., & Otto, P. A. (2007). Maximum likelyhood estimates of penetrance: a pilot study using the ectrodactyly-hemimelia syndrome. In Resumo. Águas de Lindóia: Instituto de Biociências, Universidade de São Paulo.
NLM
Horimoto ARVR, Lezirovitz K, Pearson PL, Otto PA. Maximum likelyhood estimates of penetrance: a pilot study using the ectrodactyly-hemimelia syndrome. Resumo. 2007 ;[citado 2025 out. 21 ]
Vancouver
Horimoto ARVR, Lezirovitz K, Pearson PL, Otto PA. Maximum likelyhood estimates of penetrance: a pilot study using the ectrodactyly-hemimelia syndrome. Resumo. 2007 ;[citado 2025 out. 21 ]
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
Fonte: 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: 21 out. 2025.
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 2025 out. 21 ] 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 2025 out. 21 ] Available from: https://doi.org/10.1159/000095922

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