Your browser doesn't support javascript.
loading
Co-inheritance of G6PD deficiency and 211 G to a variation of UGT1A1 in neonates with hyperbilirubinemia in eastern Guangdong.
Xu, Jia-Xin; Lin, Fen; Chen, Zi-Kai; Luo, Zhao-Yun; Zhan, Xiao-Fen; Wu, Jiao-Ren; Ma, Yu-Bin; Li, Jian-Dong; Yang, Li-Ye.
Afiliación
  • Xu JX; Central Laboratory, Chaozhou Central Hospital Affiliated to Southern Medical University, Chaozhou, 521021, Guangdong Province, People's Republic of China.
  • Lin F; Central Laboratory, Chaozhou Central Hospital Affiliated to Southern Medical University, Chaozhou, 521021, Guangdong Province, People's Republic of China.
  • Chen ZK; School of Food Engineering and Biotechnology, Hanshan Normal University, Chaozhou, 521021, Guangdong Province, People's Republic of China.
  • Luo ZY; Central Laboratory, Chaozhou Central Hospital Affiliated to Southern Medical University, Chaozhou, 521021, Guangdong Province, People's Republic of China.
  • Zhan XF; Central Laboratory, Chaozhou Central Hospital Affiliated to Southern Medical University, Chaozhou, 521021, Guangdong Province, People's Republic of China.
  • Wu JR; Central Laboratory, Chaozhou Central Hospital Affiliated to Southern Medical University, Chaozhou, 521021, Guangdong Province, People's Republic of China.
  • Ma YB; Department of Pediatrics, Chaozhou Central Hospital Affiliated to Southern Medical University, Chaozhou, 521021, Guangdong Province, People's Republic of China.
  • Li JD; Department of Pediatrics, Chaozhou Central Hospital Affiliated to Southern Medical University, Chaozhou, 521021, Guangdong Province, People's Republic of China.
  • Yang LY; Precision Medical Center, People's Hospital of Yangjiang Affiliated to Guangdong Medical University, No. 42 Dongshan Road, Yangjiang, 529500, Guangdong Province, People's Republic of China. yangleeyee@sina.com.
BMC Pediatr ; 21(1): 564, 2021 12 11.
Article en En | MEDLINE | ID: mdl-34895177
Asunto(s)
Palabras clave
Texto completo
Añadir a Mi BVS
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Glucuronosiltransferasa / Hiperbilirrubinemia Neonatal / Deficiencia de Glucosafosfato Deshidrogenasa Tipo de estudio: Observational_studies Límite: Humans / Newborn Idioma: En Revista: BMC Pediatr Asunto de la revista: PEDIATRIA Año: 2021 Tipo del documento: Article
Texto completo
Añadir a Mi BVS
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Glucuronosiltransferasa / Hiperbilirrubinemia Neonatal / Deficiencia de Glucosafosfato Deshidrogenasa Tipo de estudio: Observational_studies Límite: Humans / Newborn Idioma: En Revista: BMC Pediatr Asunto de la revista: PEDIATRIA Año: 2021 Tipo del documento: Article