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Mutational spectrum of CENP-B box and α-satellite DNA on chromosome 21 in Down syndrome children.
Chen, Qian; Tan, Bin; He, Jun-Lin; Liu, Xue-Qing; Chen, Xue-Mei; Gao, Ru-Fei; Zhu, Jing; Wang, Ying-Xiong; Qi, Hong-Bo.
Afiliação
  • Chen Q; Department of Obstetrics and Gynecology, The First Affiliated Hospital of Chongqing Medical University, Chongqing 400016, P.R. China.
  • Tan B; Pediatrics Research Institute, Children's Hospital of Chongqing Medical University, Ministry of Education Key Laboratory of Child Development and Disorders, Chongqing 400014, P.R. China.
  • He JL; Laboratory of Reproductive Biology, Public Health College, Chongqing Medical University, Chongqing 400016, P.R. China.
  • Liu XQ; Laboratory of Reproductive Biology, Public Health College, Chongqing Medical University, Chongqing 400016, P.R. China.
  • Chen XM; Laboratory of Reproductive Biology, Public Health College, Chongqing Medical University, Chongqing 400016, P.R. China.
  • Gao RF; Laboratory of Reproductive Biology, Public Health College, Chongqing Medical University, Chongqing 400016, P.R. China.
  • Zhu J; Pediatrics Research Institute, Children's Hospital of Chongqing Medical University, Ministry of Education Key Laboratory of Child Development and Disorders, Chongqing 400014, P.R. China.
  • Wang YX; Laboratory of Reproductive Biology, Public Health College, Chongqing Medical University, Chongqing 400016, P.R. China.
  • Qi HB; Department of Obstetrics and Gynecology, The First Affiliated Hospital of Chongqing Medical University, Chongqing 400016, P.R. China.
Mol Med Rep ; 15(4): 2313-2317, 2017 Apr.
Article em En | MEDLINE | ID: mdl-28259924
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Cromossomos Humanos Par 21 / DNA Satélite / Síndrome de Down / Proteína B de Centrômero / Mutação Tipo de estudo: Risk_factors_studies Limite: Child / Humans País/Região como assunto: Asia Idioma: En Revista: Mol Med Rep Ano de publicação: 2017 Tipo de documento: Article
Texto completo
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PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Cromossomos Humanos Par 21 / DNA Satélite / Síndrome de Down / Proteína B de Centrômero / Mutação Tipo de estudo: Risk_factors_studies Limite: Child / Humans País/Região como assunto: Asia Idioma: En Revista: Mol Med Rep Ano de publicação: 2017 Tipo de documento: Article