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1.
Clinical features of children with lysinuric protein intolerance and SLC7A7 gene mutation: an analysis of 3 cases / 中国当代儿科杂志
Chinese Journal of Contemporary Pediatrics
; (12): 375-380, 2019.
Artículo
en Zh
| WPRIM | ID: wpr-774068
2.
Clinical features and genetic analysis of a case with carnitine palmitoyltransferase 1A deficiency / 中华医学遗传学杂志
Chinese Journal of Medical Genetics
; (6): 228-231, 2017.
Artículo
en Zh
| WPRIM | ID: wpr-335149
3.
Effects of SMYD3 and MLL5 on histone methylation of Foxp3 gene in children with Kawasaki disease / 中华风湿病学杂志
Chinese Journal of Rheumatology
; (12): 518-523, 2017.
Artículo
en Zh
| WPRIM | ID: wpr-613147
4.
The SLC22A5 genetic analysis in Chinese patients with systemic primary carnitine deficiency / 中华内分泌代谢杂志
Chinese Journal of Endocrinology and Metabolism
; (12): 208-214, 2017.
Artículo
en Zh
| WPRIM | ID: wpr-513580
5.
Role of ash2 (absent, small, or homeotic)-like and Jumonji domain-containing protein 3 on histone methylation of interferon-gamma gene and their associations with vascular damage of Kawasaki disease / 中华心血管病杂志
Chinese Journal of Cardiology
; (12): 791-798, 2017.
Artículo
en Zh
| WPRIM | ID: wpr-809254
6.
Effects of p300/CBP on histone acetylation of Foxp3 gene in children with Kawasaki disease / 中华微生物学和免疫学杂志
Chinese Journal of Microbiology and Immunology
; (12): 347-354, 2017.
Artículo
en Zh
| WPRIM | ID: wpr-612658
7.
Changes and significances of IL-17-associated histone methylation in the acute phase of Kawasaki dis-ease / 中华微生物学和免疫学杂志
Chinese Journal of Microbiology and Immunology
; (12): 692-698, 2016.
Artículo
en Zh
| WPRIM | ID: wpr-504269
8.
Analysis of L2HGDH gene mutation in a patient with 2-hydroxyglutaric aciduria / 中华医学遗传学杂志
Chinese Journal of Medical Genetics
; (6): 48-52, 2016.
Artículo
en Zh
| WPRIM | ID: wpr-247738
9.
Analysis of clinical phenotype and ACAT1 gene mutation in a family affected with beta-ketothiolase deficiency / 中华医学遗传学杂志
Chinese Journal of Medical Genetics
; (6): 286-291, 2016.
Artículo
en Zh
| WPRIM | ID: wpr-247689
10.
Analysis of MUT gene mutations in a patient with isolated methylmalonic acidemia / 中华医学遗传学杂志
Chinese Journal of Medical Genetics
; (6): 218-221, 2015.
Artículo
en Zh
| WPRIM | ID: wpr-239501
11.
Suppurative arthritis caused by Gemella morbillorum in a patient with rheumatoid arthritis of the knee / 南方医科大学学报
Journal of Southern Medical University
; (12): 437-438, 2012.
Artículo
en Zh
| WPRIM | ID: wpr-267580
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