Association between the rs2288947 polymorphism of the lncRNA TINCR gene and the risk of recurrent miscarriage in a Southern Chinese population.

Huang, Wendong; Zhou, Huazhong; Pi, Lei; Xu, Yufen; Fu, LanYan; Yang, Yanfang; Che, Di; Gu, Xiaoqiong

Huang, Wendong; Zhou, Huazhong; Pi, Lei; Xu, Yufen; Fu, LanYan; Yang, Yanfang; Che, Di; Gu, Xiaoqiong.

Afiliação

Huang W; Department of Pharmacy, Maoming People's Hospital, Maoming, China.
Zhou H; Department of Clinical Biological Resource Bank, Guangzhou Institute of Pediatrics, Guangzhou Women and Children's Medical Center, Guangzhou Medical University, Guangzhou, China.
Pi L; Department of Clinical Biological Resource Bank, Guangzhou Institute of Pediatrics, Guangzhou Women and Children's Medical Center, Guangzhou Medical University, Guangzhou, China.
Xu Y; Department of Clinical Biological Resource Bank, Guangzhou Institute of Pediatrics, Guangzhou Women and Children's Medical Center, Guangzhou Medical University, Guangzhou, China.
Fu L; Department of Clinical Biological Resource Bank, Guangzhou Institute of Pediatrics, Guangzhou Women and Children's Medical Center, Guangzhou Medical University, Guangzhou, China.
Yang Y; Department of Prenatal Diagnosis, Maoming People's Hospital, Maoming, China.
Che D; Department of Clinical Biological Resource Bank, Guangzhou Institute of Pediatrics, Guangzhou Women and Children's Medical Center, Guangzhou Medical University, Guangzhou, China.
Gu X; Department of Clinical Biological Resource Bank, Guangzhou Institute of Pediatrics, Guangzhou Women and Children's Medical Center, Guangzhou Medical University, Guangzhou, China.

J Clin Lab Anal ; 33(6): e22919, 2019 Jul.

Article em En | MEDLINE | ID: mdl-31124188

Assuntos

Aborto Habitual/genética; Polimorfismo de Nucleotídeo Único; RNA Longo não Codificante/genética; Adulto; Povo Asiático/genética; Estudos de Casos e Controles; Feminino; Frequência do Gene; Predisposição Genética para Doença; Humanos

Palavras-chave

genetic susceptibility; lncRNA TINCR; recurrent miscarriage

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Aborto Habitual / Polimorfismo de Nucleotídeo Único / RNA Longo não Codificante Tipo de estudo: Clinical_trials / Etiology_studies / Observational_studies / Risk_factors_studies Limite: Adult / Female / Humans Idioma: En Revista: J Clin Lab Anal Assunto da revista: TECNICAS E PROCEDIMENTOS DE LABORATORIO Ano de publicação: 2019 Tipo de documento: Article País de afiliação: China País de publicação: Estados Unidos

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