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Chinese Journal of Pediatrics

Issue 11, 2018

Items 1-5 of 19

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婴儿肝功能衰竭综合征2型一例

Chinese Journal of Pediatrics, Volume 56, Issue 11,2018, Pages 876-877, doi:10.3760/cma.j.issn.0578-1310.2018.11.018

A family with Allan-Herndon-Dudley syndrome due to SLC16A2 gene mutation

Chinese Journal of Pediatrics, Volume 56, Issue 11,2018, Pages 829-834, doi:10.3760/cma.j.issn.0578-1310.2018.11.008

Genetic and clinical analysis of children with early-onset epilepsy encephalopathy caused by KCNT1 gene mutation

Chinese Journal of Pediatrics, Volume 56, Issue 11,2018, Pages 824-828, doi:10.3760/cma.j.issn.0578-1310.2018.11.007

Clinical and laboratory characteristics and genetic diagnosis of Kabuki syndrome

Chinese Journal of Pediatrics, Volume 56, Issue 11,2018, Pages 846-849, doi:10.3760/cma.j.issn.0578-1310.2018.11.010

医患共同决策在儿科中的应用进展

Chinese Journal of Pediatrics, Volume 56, Issue 11,2018, Pages 878-880, doi:10.3760/cma.j.issn.0578-1310.2018.11.019

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