Assessment of CDKN1C gene in patients with hypertensive disorders of pregnancy (2010)
- Authors:
- USP affiliated authors: RAMOS, ESTER SILVEIRA - FMRP ; SILVA JUNIOR, WILSON ARAÚJO DA - FMRP ; DUARTE, GERALDO - FMRP ; GOLDMAN, MARIA HELENA DE SOUZA - FFCLRP
- Unidades: FMRP; FFCLRP
- Subjects: HIPERTENSÃO NA GRAVIDEZ; GENÉTICA
- Language: Inglês
- Imprenta:
- Publisher: FMRP/USP
- Publisher place: Ribeirão Preto
- Date published: 2010
- Source:
- Título: Abstracts Book
- Conference titles: Workshop do Programa de Pós-Graduação em Genética Básica, Genética Humana e Médica e Bioinformática
-
ABNT
SOARES, M. R. et al. Assessment of CDKN1C gene in patients with hypertensive disorders of pregnancy. 2010, Anais.. Ribeirão Preto: FMRP/USP, 2010. . Acesso em: 06 nov. 2024. -
APA
Soares, M. R., Araújo, F. M., Kaneto, C. M., Galerani, M. A. V., Ferreira, C. A., Marques, A. A., et al. (2010). Assessment of CDKN1C gene in patients with hypertensive disorders of pregnancy. In Abstracts Book. Ribeirão Preto: FMRP/USP. -
NLM
Soares MR, Araújo FM, Kaneto CM, Galerani MAV, Ferreira CA, Marques AA, Quiapim AC, Goldman MH de S, Duarte G, Silva Júnior WA, Ramos ES. Assessment of CDKN1C gene in patients with hypertensive disorders of pregnancy. Abstracts Book. 2010 ;[citado 2024 nov. 06 ] -
Vancouver
Soares MR, Araújo FM, Kaneto CM, Galerani MAV, Ferreira CA, Marques AA, Quiapim AC, Goldman MH de S, Duarte G, Silva Júnior WA, Ramos ES. Assessment of CDKN1C gene in patients with hypertensive disorders of pregnancy. Abstracts Book. 2010 ;[citado 2024 nov. 06 ] - Pesquisa de variantes do gene CDKN1C em pacientes portadoras de síndromes hipertensivas gestacionais
- New variants in the imprinted CDKN1C gene
- Avaliação da influência dos polimorfismos H19/RsaI e IGF2/ApaI no peso da placenta de pacientes com Síndromes Hipertensivas Gestacionais
- The KvDMR1 and H19DMR methylation pattern in placenta of patients with preeclampsia
- Hydroxymethylation versus methylation in an imprinted region of the human placenta
- Hydroxymethylation versus methylation in an imprinted region of the human placenta
- New CDKN1C gene variants in the Beckwith-Wiedemann syndrome
- Padrão de expressão de microRNAs X-específicos na pré-eclâmpsia
- Placental hydroxymethylation vs methylation at the imprinting control region 2 on chromosome 11p15.5
- DMR study, genic expression and genomic variants in preeclamptic Women
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