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Comprehensive Analysis of Fragile X Syndrome: Full Characterization of the FMR1 Locus by Long-Read Sequencing.
Liang, Qiaowei; Liu, Yingdi; Liu, Yaning; Duan, Ranhui; Meng, Wanli; Zhan, Jiahan; Xia, Jiahui; Mao, Aiping; Liang, Desheng; Wu, Lingqian.
Afiliación
  • Liang Q; Department of Medical Genetics, Hunan Jiahui Genetics Hospital, Changsha, Hunan, China.
  • Liu Y; Center for Medical Genetics and Hunan Key Laboratory of Medical Genetics, School of Life Sciences, Central South University, Changsha, Hunan, China.
  • Liu Y; Department of Medical Genetics, Hunan Jiahui Genetics Hospital, Changsha, Hunan, China.
  • Duan R; Center for Medical Genetics and Hunan Key Laboratory of Medical Genetics, School of Life Sciences, Central South University, Changsha, Hunan, China.
  • Meng W; Berry Genomics Corporation, Beijing, China.
  • Zhan J; Berry Genomics Corporation, Beijing, China.
  • Xia J; Department of Medical Genetics, Hunan Jiahui Genetics Hospital, Changsha, Hunan, China.
  • Mao A; Berry Genomics Corporation, Beijing, China.
  • Liang D; Department of Medical Genetics, Hunan Jiahui Genetics Hospital, Changsha, Hunan, China.
  • Wu L; Center for Medical Genetics and Hunan Key Laboratory of Medical Genetics, School of Life Sciences, Central South University, Changsha, Hunan, China.
Clin Chem ; 68(12): 1529-1540, 2022 12 06.
Article en En | MEDLINE | ID: mdl-36171182
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Síndrome del Cromosoma X Frágil Tipo de estudio: Diagnostic_studies / Prognostic_studies Idioma: En Revista: Clin Chem Asunto de la revista: QUIMICA CLINICA Año: 2022 Tipo del documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Síndrome del Cromosoma X Frágil Tipo de estudio: Diagnostic_studies / Prognostic_studies Idioma: En Revista: Clin Chem Asunto de la revista: QUIMICA CLINICA Año: 2022 Tipo del documento: Article