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1.
Clinical phenotype and genetic analysis of MED13L syndrome / 中国当代儿科杂志
Chinese Journal of Contemporary Pediatrics
; (12): 1083-1086, 2017.
Artículo
en Zh
| WPRIM | ID: wpr-300444
2.
Association of mammalian target of rapamycin gene polymorphisms with the risk of pediatric epilepsy / 中国当代儿科杂志
Chinese Journal of Contemporary Pediatrics
; (12): 560-564, 2015.
Artículo
en Zh
| WPRIM | ID: wpr-346106
3.
Association of HLA-B*1502 and *1511 allele with antiepileptic drug-induced Stevens-Johnson syndrome in central China / 华中科技大学学报(医学)(英德文版)
Journal of Huazhong University of Science and Technology (Medical Sciences)
; (6): 146-50, 2014.
Artículo
en Inglés
| WPRIM | ID: wpr-636526
4.
Association of HLA-B*1502 and *1511 allele with antiepileptic drug-induced Stevens-Johnson syndrome in central China / 华中科技大学学报(医学)(英德文版)
Journal of Huazhong University of Science and Technology (Medical Sciences)
; (6): 146-150, 2014.
Artículo
en Inglés
| WPRIM | ID: wpr-351107
5.
Clinical features and MECP2 mutations in children with Rett syndrome / 中国当代儿科杂志
Chinese Journal of Contemporary Pediatrics
; (12): 393-396, 2014.
Artículo
en Zh
| WPRIM | ID: wpr-269465
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