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A very rare case of trisomy 4q32.3-4q35.2 and trisomy 21q11.2-21q22.11 in a patient with recombinant chromosomes 4 and 21.
Chen, Li-Sha; Xue, Dan; Xi, Zuo-Ming; Liu, Dan-Na; Zou, Peng-Shu; Ma, Ming; Xia, Ying; Chen, Xia-Hui; Qiu, Guang-Bin; Cao, Dong-Hua.
Afiliação
  • Chen LS; Aristogenesis Center, No. 202 Hospital of PLA, Shenyang 110003, PR China.
  • Xue D; Aristogenesis Center, No. 202 Hospital of PLA, Shenyang 110003, PR China.
  • Xi ZM; Genetic disease laboratory, DongChang Maternal and Child Health Hospital, LiaoCheng 252000, PR China.
  • Liu DN; Aristogenesis Center, No. 202 Hospital of PLA, Shenyang 110003, PR China.
  • Zou PS; Aristogenesis Center, No. 202 Hospital of PLA, Shenyang 110003, PR China.
  • Ma M; Aristogenesis Center, No. 202 Hospital of PLA, Shenyang 110003, PR China.
  • Xia Y; Aristogenesis Center, No. 202 Hospital of PLA, Shenyang 110003, PR China.
  • Chen XH; Aristogenesis Center, No. 202 Hospital of PLA, Shenyang 110003, PR China.
  • Qiu GB; Department of Laboratory Medicine, No. 202 Hospital of PLA, Shenyang 110003, PR China.
  • Cao DH; Aristogenesis Center, No. 202 Hospital of PLA, Shenyang 110003, PR China. Electronic address: dhcao427@sina.com.
Gene ; 563(1): 72-5, 2015 May 25.
Article em En | MEDLINE | ID: mdl-25752286
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Trissomia / Síndrome de Down / Deficiência Intelectual Tipo de estudo: Prognostic_studies Limite: Adult / Female / Humans Idioma: En Revista: Gene Ano de publicação: 2015 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Trissomia / Síndrome de Down / Deficiência Intelectual Tipo de estudo: Prognostic_studies Limite: Adult / Female / Humans Idioma: En Revista: Gene Ano de publicação: 2015 Tipo de documento: Article