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1.
A case of dilated cardiomyopathy caused by FHL2 gene variant and a literature review / 中华医学遗传学杂志
Chinese Journal of Medical Genetics
; (6): 337-343, 2023.
Artículo
en Zh
| WPRIM | ID: wpr-970929
2.
Clinical and genetic analysis of eight children with Primary hypertrophic cardiomyopathy / 中华医学遗传学杂志
Chinese Journal of Medical Genetics
; (6): 1211-1216, 2023.
Artículo
en Zh
| WPRIM | ID: wpr-1009277
3.
The Diagnosis and Treatment of Rare Diseases in Children: Now and Future / 罕见病研究
JOURNAL OF RARE DISEASES
; (4): 229-232, 2022.
Artículo
en Inglés
| WPRIM | ID: wpr-1005008
4.
Mental retardation autosomal dominant 35 caused by de novo missense variants in PPP2R5D gene: a case report and literature review / 中华神经科杂志
Chinese Journal of Neurology
; (12): 1286-1291, 2022.
Artículo
en Zh
| WPRIM | ID: wpr-958026
5.
Identification of variants in TNNI3 gene in two children with restrictive cardiomyopathy / 中华医学遗传学杂志
Chinese Journal of Medical Genetics
; (6): 731-734, 2021.
Artículo
en Zh
| WPRIM | ID: wpr-888382
6.
Long-term prognosis of allergic bronchopulmonary aspergillosis in children with cystic fibrosis / 中华实用儿科临床杂志
Chinese Journal of Applied Clinical Pediatrics
; (24): 949-953, 2021.
Artículo
en Zh
| WPRIM | ID: wpr-907878
7.
Analysis of SMARCA2 gene mutation in a child with Nicolaides-Baraitser syndrome / 中华医学遗传学杂志
Chinese Journal of Medical Genetics
; (6): 1187-1190, 2019.
Artículo
en Zh
| WPRIM | ID: wpr-799973
8.
Analysis of SMARCA2 gene mutation in a child with Nicolaides-Baraitser syndrome / 中华医学遗传学杂志
Chinese Journal of Medical Genetics
; (6): 1187-1190, 2019.
Artículo
en Zh
| WPRIM | ID: wpr-781320
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