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1.
Structural characteristics of lower respiratory tract microflora in patients with pneumoconiosis / 中华劳动卫生职业病杂志
Chinese Journal of Industrial Hygiene and Occupational Diseases
; (12): 247-254, 2023.
Artículo
en Zh
| WPRIM | ID: wpr-986023
2.
Advances in quality research of Cinnamomum cassia / 中国中药杂志
China Journal of Chinese Materia Medica
; (24): 2792-2799, 2020.
Artículo
en Zh
| WPRIM | ID: wpr-828082
3.
Off-ladder Alleles Detected by Expressmarker22 Kit in Guangdong Han Population / 中山大学学报(医学科学版)
Journal of Sun Yat-sen University(Medical Sciences)
; (6): 227-232, 2018.
Artículo
en Zh
| WPRIM | ID: wpr-712938
4.
Genetic Polymorphisms of SNP Located in the 5' Region of VEGF Gene in Han Population in Guangdong / 法医学杂志
Journal of Forensic Medicine
; (6): 257-260, 2016.
Artículo
en Zh
| WPRIM | ID: wpr-984842
5.
SNP in Differentially Methylated Region Upstream of H19 Gene in Guangdong Han Population / 法医学杂志
Journal of Forensic Medicine
; (6): 184-188, 2016.
Artículo
en Inglés
| WPRIM | ID: wpr-984832
6.
Clinical value of cranial MRI in the diagnosis and treatment of central nervous system candidiasis / 中国当代儿科杂志
Chinese Journal of Contemporary Pediatrics
; (12): 834-839, 2014.
Artículo
en Zh
| WPRIM | ID: wpr-254188
7.
Detection of aberrant PTPRO gene methylation in peripheral blood and its clinical significance in breast cancer patients / 肿瘤
Tumor
; (12): 1087-1094, 2013.
Artículo
en Zh
| WPRIM | ID: wpr-848896
8.
Diagnosis and treatment of group A β-hemolytic Streptococcal pharyngitis / 中华实用儿科临床杂志
Chinese Journal of Applied Clinical Pediatrics
; (24): 1751-1752, 2013.
Artículo
en Zh
| WPRIM | ID: wpr-733219
9.
Analysis of de novo copy number variations in a family affected with autism spectrum disorders using high-resolution array-based comparative genomic hybridization / 中华医学遗传学杂志
Chinese Journal of Medical Genetics
; (6): 266-269, 2012.
Artículo
en Zh
| WPRIM | ID: wpr-295497
10.
PIK3CA mutation is an independent indicator of malignant phenotype and prognosis in breast cancer / 中华肿瘤杂志
Chinese Journal of Oncology
; (12): 605-608, 2011.
Artículo
en Zh
| WPRIM | ID: wpr-320161
11.
A survey on the standardized treatment of 33 cases of children thalassemia and their family economic burden in Bao'an district, Shenzhen city, 2009 / 中国地方病学杂志
Chinese Journal of Endemiology
; (6): 332-335, 2011.
Artículo
en Zh
| WPRIM | ID: wpr-643248
12.
Study of dystrophin gene non-deletion/duplication mutations causing Becker muscular dystrophy / 中华医学遗传学杂志
Chinese Journal of Medical Genetics
; (6): 308-312, 2011.
Artículo
en Zh
| WPRIM | ID: wpr-326940
13.
Development and genetic polymorphism of abnormal pronuclear zygotes after intracytoplasmic sperm injection / 中华医学遗传学杂志
Chinese Journal of Medical Genetics
; (6): 410-413, 2010.
Artículo
en Zh
| WPRIM | ID: wpr-234394
14.
Identification of deletion/duplication mutations in DMD gene by multiple ligation probe amplification and denaturing high-performance liquid chromatography / 中国医学科学院学报
Acta Academiae Medicinae Sinicae
; (6): 83-86, 2007.
Artículo
en Zh
| WPRIM | ID: wpr-230027
15.
Detection of genomic duplications and deletions of the DMD gene in affected males and female carriers by using mutiplex ligation-dependent probe amplification / 中华医学遗传学杂志
Chinese Journal of Medical Genetics
; (6): 460-463, 2007.
Artículo
en Zh
| WPRIM | ID: wpr-247292
16.
Sibling brother and sister both with Duchenne muscular dystrophy / 中国医学科学院学报
Acta Academiae Medicinae Sinicae
; (6): 543-547, 2007.
Artículo
en Zh
| WPRIM | ID: wpr-229937
17.
Identification of disease-causing point mutations in DMD patients' dystrophin gene without large deletions/duplications / 中华医学遗传学杂志
Chinese Journal of Medical Genetics
; (6): 392-396, 2006.
Artículo
en Zh
| WPRIM | ID: wpr-263770
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