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Development a multiplex panel of AISNPs, multi-allelic InDels, microhaplotypes, and Y-SNP/InDel loci for multiple forensic purposes via the NGS.
Jin, Xiao-Ye; Liu, Yan-Fang; Cui, Wei; Chen, Chong; Zhang, Xing-Ru; Huang, Jiang; Zhu, Bo-Feng.
Afiliação
  • Jin XY; Key Laboratory of Shaanxi Province for Craniofacial Precision Medicine Research, College of Stomatology, Xi'an Jiaotong University, Xi'an, P. R. China.
  • Liu YF; Department of Forensic Medicine, Guizhou Medical University, Guiyang, P. R. China.
  • Cui W; Guangzhou Key Laboratory of Forensic Multi-Omics for Precision Identification, School of Forensic Medicine, Southern Medical University, Guangzhou, P. R. China.
  • Chen C; Guangzhou Key Laboratory of Forensic Multi-Omics for Precision Identification, School of Forensic Medicine, Southern Medical University, Guangzhou, P. R. China.
  • Zhang XR; Key Laboratory of Shaanxi Province for Craniofacial Precision Medicine Research, College of Stomatology, Xi'an Jiaotong University, Xi'an, P. R. China.
  • Huang J; Key Laboratory of Shaanxi Province for Craniofacial Precision Medicine Research, College of Stomatology, Xi'an Jiaotong University, Xi'an, P. R. China.
  • Zhu BF; Department of Forensic Medicine, Guizhou Medical University, Guiyang, P. R. China.
Electrophoresis ; 43(4): 632-644, 2022 02.
Article em En | MEDLINE | ID: mdl-34859475
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Polimorfismo de Nucleotídeo Único / Mutação INDEL Limite: Humans País/Região como assunto: Asia Idioma: En Ano de publicação: 2022 Tipo de documento: Article
Texto completo
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XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Polimorfismo de Nucleotídeo Único / Mutação INDEL Limite: Humans País/Região como assunto: Asia Idioma: En Ano de publicação: 2022 Tipo de documento: Article