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Population-based carrier screening and prenatal diagnosis of fragile X syndrome in East Asian populations.
Guo, Qiwei; Chang, Yih-Yuan; Huang, Chien-Hao; Hsiao, Yu-Shan; Hsiao, Yu-Chiao; Chiu, I-Fan; Zhou, Yulin; Zhang, Haixia; Ko, Tsang-Ming.
Afiliación
  • Guo Q; United Diagnostic and Research Center for Clinical Genetics, Women and Children's Hospital, School of Medicine & School of Public Health, Xiamen University, Xiamen, Fujian 361102, China. Electronic address: guoqiwei@xmu.edu.cn.
  • Chang YY; Genephile Bioscience Laboratory, Ko's Obstetrics and Gynecology, Taipei 100, Taiwan, China.
  • Huang CH; Genephile Bioscience Laboratory, Ko's Obstetrics and Gynecology, Taipei 100, Taiwan, China.
  • Hsiao YS; Genephile Bioscience Laboratory, Ko's Obstetrics and Gynecology, Taipei 100, Taiwan, China.
  • Hsiao YC; Biofast Biotechnology Co., Ltd., Xiamen, Fujian 361102, China.
  • Chiu IF; Biofast Biotechnology Co., Ltd., Xiamen, Fujian 361102, China.
  • Zhou Y; United Diagnostic and Research Center for Clinical Genetics, Women and Children's Hospital, School of Medicine & School of Public Health, Xiamen University, Xiamen, Fujian 361102, China.
  • Zhang H; United Diagnostic and Research Center for Clinical Genetics, Women and Children's Hospital, School of Medicine & School of Public Health, Xiamen University, Xiamen, Fujian 361102, China.
  • Ko TM; Genephile Bioscience Laboratory, Ko's Obstetrics and Gynecology, Taipei 100, Taiwan, China. Electronic address: ko.obs@msa.hinet.net.
J Genet Genomics ; 48(12): 1104-1110, 2021 12.
Article en En | MEDLINE | ID: mdl-34412977
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Síndrome del Cromosoma X Frágil Tipo de estudio: Diagnostic_studies / Prognostic_studies / Risk_factors_studies / Screening_studies Límite: Adult / Female / Humans / Pregnancy Idioma: En Revista: J Genet Genomics Año: 2021 Tipo del documento: Article Pais de publicación: China
Texto completo
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Síndrome del Cromosoma X Frágil Tipo de estudio: Diagnostic_studies / Prognostic_studies / Risk_factors_studies / Screening_studies Límite: Adult / Female / Humans / Pregnancy Idioma: En Revista: J Genet Genomics Año: 2021 Tipo del documento: Article Pais de publicación: China