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Filtros : "Der Kaloustian, Vazken M." Limpar

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Trabalho de evento-resumo periodico
Endostatin measurement as preliminary screening test for the diagnosis of Knobloch syndrome (2002)
Suzuki, Oscar T.; Kok, Fernando; Der Kaloustian, Vazken M.; Olsen, Björn
Fonte: Abstracts. Nome do evento: Annual Meeting of the American Society of Human Genetics. Unidade: IB
Assunto: DOENÇAS GENÉTICAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SUZUKI, Oscar T. et al. Endostatin measurement as preliminary screening test for the diagnosis of Knobloch syndrome. Abstracts. Baltimore: Instituto de Biociências, Universidade de São Paulo. . Acesso em: 10 nov. 2024. , 2002
APA
Suzuki, O. T., Kok, F., Der Kaloustian, V. M., & Olsen, B. (2002). Endostatin measurement as preliminary screening test for the diagnosis of Knobloch syndrome. Abstracts. Baltimore: Instituto de Biociências, Universidade de São Paulo.
NLM
Suzuki OT, Kok F, Der Kaloustian VM, Olsen B. Endostatin measurement as preliminary screening test for the diagnosis of Knobloch syndrome. Abstracts. 2002 ; 71( 4): 287 res.678.[citado 2024 nov. 10 ]
Vancouver
Suzuki OT, Kok F, Der Kaloustian VM, Olsen B. Endostatin measurement as preliminary screening test for the diagnosis of Knobloch syndrome. Abstracts. 2002 ; 71( 4): 287 res.678.[citado 2024 nov. 10 ]
Artigo de periodico
Molecular analysis of collagen XVIII reveals novel mutations, presence of a third isoform, and possible genetic heterogeneity in Knobloch syndrome (2002)
Suzuki, Oscar T.; Sertié, Andréa Laurato; Der Kaloustian, Vazken M.; Kok, Fernando; Carpenter, M.; Murray, J; Czeizel, A E; Kliemann, Susana E.; Rosemberg, Sérgio; Monteiro, M.; Olsen, Bjorn Reino; Passos-Bueno, Maria Rita
Fonte: American Journal of Human Genetics. Unidades: IB, FM
Assuntos: DEGENERAÇÃO RETINIANA, DOENÇAS RETINIANAS, CEGUEIRA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SUZUKI, Oscar T. et al. Molecular analysis of collagen XVIII reveals novel mutations, presence of a third isoform, and possible genetic heterogeneity in Knobloch syndrome. American Journal of Human Genetics, v. 71, p. 1320-1329, 2002Tradução . . Acesso em: 10 nov. 2024.
APA
Suzuki, O. T., Sertié, A. L., Der Kaloustian, V. M., Kok, F., Carpenter, M., Murray, J., et al. (2002). Molecular analysis of collagen XVIII reveals novel mutations, presence of a third isoform, and possible genetic heterogeneity in Knobloch syndrome. American Journal of Human Genetics, 71, 1320-1329.
NLM
Suzuki OT, Sertié AL, Der Kaloustian VM, Kok F, Carpenter M, Murray J, Czeizel AE, Kliemann SE, Rosemberg S, Monteiro M, Olsen BR, Passos-Bueno MR. Molecular analysis of collagen XVIII reveals novel mutations, presence of a third isoform, and possible genetic heterogeneity in Knobloch syndrome. American Journal of Human Genetics. 2002 ; 71 1320-1329.[citado 2024 nov. 10 ]
Vancouver
Suzuki OT, Sertié AL, Der Kaloustian VM, Kok F, Carpenter M, Murray J, Czeizel AE, Kliemann SE, Rosemberg S, Monteiro M, Olsen BR, Passos-Bueno MR. Molecular analysis of collagen XVIII reveals novel mutations, presence of a third isoform, and possible genetic heterogeneity in Knobloch syndrome. American Journal of Human Genetics. 2002 ; 71 1320-1329.[citado 2024 nov. 10 ]

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