ReP USP - Resultado da busca

Artigo de periodico
Typical phenotypic spectrum of velocardiofacial syndrome occurs independently of deletion size in chromosome 22q11.2 (2007)
Sandrin-Garcia, Paula; Abramides, Dagma Venturini Marques; Martelli, Lúcia Regina; Ramos, Ester Silveira; Richieri-Costa, Antonio; Passos, Geraldo Aleixo Silva
Source: Molecular and Cellular Biochemistry. Unidades: FOB, FMRP, HRAC, FORP
Subjects: ANORMALIDADES MÚLTIPLAS, ANORMALIDADES CRANIOFACIAIS, FENÓTIPOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SANDRIN-GARCIA, Paula et al. Typical phenotypic spectrum of velocardiofacial syndrome occurs independently of deletion size in chromosome 22q11.2. Molecular and Cellular Biochemistry, v. 303, n. 1/2, p. 9-17, 2007Tradução . . Disponível em: https://doi.org/10.1007/s11010-007-9450-5. Acesso em: 12 nov. 2024.
APA
Sandrin-Garcia, P., Abramides, D. V. M., Martelli, L. R., Ramos, E. S., Richieri-Costa, A., & Passos, G. A. S. (2007). Typical phenotypic spectrum of velocardiofacial syndrome occurs independently of deletion size in chromosome 22q11.2. Molecular and Cellular Biochemistry, 303( 1/2), 9-17. doi:10.1007/s11010-007-9450-5
NLM
Sandrin-Garcia P, Abramides DVM, Martelli LR, Ramos ES, Richieri-Costa A, Passos GAS. Typical phenotypic spectrum of velocardiofacial syndrome occurs independently of deletion size in chromosome 22q11.2 [Internet]. Molecular and Cellular Biochemistry. 2007 ; 303( 1/2): 9-17.[citado 2024 nov. 12 ] Available from: https://doi.org/10.1007/s11010-007-9450-5
Vancouver
Sandrin-Garcia P, Abramides DVM, Martelli LR, Ramos ES, Richieri-Costa A, Passos GAS. Typical phenotypic spectrum of velocardiofacial syndrome occurs independently of deletion size in chromosome 22q11.2 [Internet]. Molecular and Cellular Biochemistry. 2007 ; 303( 1/2): 9-17.[citado 2024 nov. 12 ] Available from: https://doi.org/10.1007/s11010-007-9450-5
Artigo de periodico
Fluorescence in situ hybridization (FISH) screening for the 22q11.2 deletion in patients with clinical features of velocardiofacial syndrome but without cardiac anomalies (2007)
Sandrin-Garcia, Paula; Richieri-Costa, Antonio; Tajara, Eloiza Helena; Carvalho-Salles, Andréa Borduchi; Fett-Conte, Agnes Cristina
Source: Genetics and Molecular Biology. Unidade: HRAC
Subjects: INSUFICIÊNCIA VELOFARÍNGEA, DELEÇÃO DE GENES, FLUORESCÊNCIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SANDRIN-GARCIA, Paula et al. Fluorescence in situ hybridization (FISH) screening for the 22q11.2 deletion in patients with clinical features of velocardiofacial syndrome but without cardiac anomalies. Genetics and Molecular Biology, v. 30, n. 1, p. 21-24, 2007Tradução . . Disponível em: https://doi.org/10.1590/s1415-47572007000100006. Acesso em: 12 nov. 2024.
APA
Sandrin-Garcia, P., Richieri-Costa, A., Tajara, E. H., Carvalho-Salles, A. B., & Fett-Conte, A. C. (2007). Fluorescence in situ hybridization (FISH) screening for the 22q11.2 deletion in patients with clinical features of velocardiofacial syndrome but without cardiac anomalies. Genetics and Molecular Biology, 30( 1), 21-24. doi:10.1590/s1415-47572007000100006
NLM
Sandrin-Garcia P, Richieri-Costa A, Tajara EH, Carvalho-Salles AB, Fett-Conte AC. Fluorescence in situ hybridization (FISH) screening for the 22q11.2 deletion in patients with clinical features of velocardiofacial syndrome but without cardiac anomalies [Internet]. Genetics and Molecular Biology. 2007 ; 30( 1): 21-24.[citado 2024 nov. 12 ] Available from: https://doi.org/10.1590/s1415-47572007000100006
Vancouver
Sandrin-Garcia P, Richieri-Costa A, Tajara EH, Carvalho-Salles AB, Fett-Conte AC. Fluorescence in situ hybridization (FISH) screening for the 22q11.2 deletion in patients with clinical features of velocardiofacial syndrome but without cardiac anomalies [Internet]. Genetics and Molecular Biology. 2007 ; 30( 1): 21-24.[citado 2024 nov. 12 ] Available from: https://doi.org/10.1590/s1415-47572007000100006
Trabalho de evento-resumo periodico
Recurrent 22q11 deletion in a sibship suggestive of parental germ-line mosaicism (1999)
Sandrin-Garcia, Paula; Martelli, Lúcia Regina; Ramos, Ester Silveira; Richieri-Costa, Antonio; Passos, Geraldo Aleixo Silva
Source: Genetics and Molecular Biology. Conference titles: Congresso Nacional de Genética. Unidades: FMRP, FORP
Assunto: GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SANDRIN-GARCIA, Paula et al. Recurrent 22q11 deletion in a sibship suggestive of parental germ-line mosaicism. Genetics and Molecular Biology. Ribeirão Preto: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. . Acesso em: 12 nov. 2024. , 1999
APA
Sandrin-Garcia, P., Martelli, L. R., Ramos, E. S., Richieri-Costa, A., & Passos, G. A. S. (1999). Recurrent 22q11 deletion in a sibship suggestive of parental germ-line mosaicism. Genetics and Molecular Biology. Ribeirão Preto: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo.
NLM
Sandrin-Garcia P, Martelli LR, Ramos ES, Richieri-Costa A, Passos GAS. Recurrent 22q11 deletion in a sibship suggestive of parental germ-line mosaicism. Genetics and Molecular Biology. 1999 ; 22( 3):[citado 2024 nov. 12 ]
Vancouver
Sandrin-Garcia P, Martelli LR, Ramos ES, Richieri-Costa A, Passos GAS. Recurrent 22q11 deletion in a sibship suggestive of parental germ-line mosaicism. Genetics and Molecular Biology. 1999 ; 22( 3):[citado 2024 nov. 12 ]

USP Schools

ReP

Filtros

Departament

Authors

Subjects

Indexado em